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Contact Lens & Anterior Eye 27 (2004) 209–212
Antimicrobial efficacy of a povidone iodine (PI) and a one-step
hydrogen peroxide contact lens disinfection system
Simon Kilvington*
Department of Infection, Immunity and Inflammation, University of Leicester, Medical Sciences Building,
P.O. Box 138, University Road, Leicester LE19HN, UK
Abstract
The antimicrobial efficacy of a novel povidone iodine (PI) contact lens disinfection system (Clencide) was compared with a one-step
hydrogen peroxide system (AoSept). The PI system showed rapid killing of organisms with a 4.5–6.0 log reduction in bacteria, yeast, mould
and Acanthamoeba trophozoites within 5 min and a 2.8–3.6 log kill of Acanthamoeba cysts after 2–4 h. The one-step peroxide gave a 4.0–6.0
log kill of bacteria in 0.5–1 h, 2.0–5.0 log for yeast after 2–6 h and 1.8 log for mould at 6 h. Acanthamoeba polyphaga trophozoites were
reduced by 3.6 log at 1 h but cysts by only 1.2 log after 6 h. The study demonstrates that the PI system is an effective disinfection method for
contact lenses.
# 2004 British Contact Lens Association. Published by Elsevier Ltd. All rights reserved.
Keywords: Povidone iodine; Hydrogen peroxide; Contact lens disinfection; Acanthamoeba
1. Introduction
Contact lens wear is a predisposing factor in some 50% of
reported cases of microbial keratitis [1–3,12]. Bacterial
keratitis is the most common form, with staphylococci,
Pseudomonas aeruginosa and Serratia spp. the usual
infectious organisms [1,2,12,22]. Although less common,
keratitis due to the free-living amoeba Acanthamoeba is
almost exclusively associated with contact lens wear, which
accounts for 90% of reported cases, with an incidence in the
UK some 15 times that of the USA and 3 times the rest of
Europe [17–19,21,23].
It has long been recognised that poor contact lens hygiene
enables microorganisms to colonise the lens storage case
[13]. This can then result in biofilm production that protects
potentially pathogenic microbes from disinfectant action
[14]. Such organisms can then adhere to the contact lenses for
inoculation on to the cornea [3,5,16]. Protein deposits also
interfere with oxygen diffusion across the lens, and other
debris on the lens surface may cause corneal abrasions
resulting in discomfort or initiation of infection [9–11,15,16]
* Tel.: +44 116 252 2950; fax: +44 116 252 5030.
E-mail address: [email protected].
1367-0484/$ – see front matter # 2004 British Contact Lens Association. Publi
doi:10.1016/j.clae.2004.09.001
thus, the regular cleaning and disinfection of contact lenses is
fundamental to both the comfort and the safety of the wearer.
Currently, contact lens disinfection is achieved through
the use of either multipurpose solutions (MPS) or hydrogen
peroxide systems. The MPS utilise a single solution for
disinfecting, rinsing and storing the lenses; with most MPS
having an inherent cleaning system.
Hydrogen peroxide (3%) is a powerful disinfectant and
has been shown to be effective against the highly resistant
cyst stage of Acanthamoeba, giving a 3 log reduction in
viability provided an exposure time of at least 4–6 h is
allowed prior to neutralisation which is essential before lens
wear to avoid pronounced discomfort and possible corneal
damage [7]. To avoid these problems and simplify use, one-
step hydrogen peroxide systems are available which do not
require separate neutralisation. Here, neutralisation is
achieved in the storage case during disinfection using a
platinum-coated disc or soluble catalase tablet which
catalyses the decomposition of hydrogen peroxide to water
and oxygen [7].
Recently, a novel povidone iodine (PI) contact lens
disinfection and cleaning system has been introduced to the
market. The system comprises a disinfectant/proteolytic
enzyme stage with simultaneous neutralisation of the PI
shed by Elsevier Ltd. All rights reserved.
S. Kilvington / Contact Lens & Anterior Eye 27 (2004) 209–212210
through the addition of a separate reagent. Disinfection and
neutralisation are complete within 10 min but the lenses are
left in the solution for at least 4 h to effect the enzymatic
cleaning. In this present study, the efficacy of the system in
comparison with a one-step hydrogen peroxide contact lens
disinfectant was evaluated for known ocular pathogenic
bacteria, fungi and Acanthamoeba.
2. Materials and methods
2.1. Test organisms
The bacteria, fungi and Acanthamoeba spp. tested were:
Pseudomonas aeruginosa (ATCC 9027), Staphylococcus
aureus (ATCC 6538), Serratia marcescens (NCTC 10211),
Candida albicans (ATCC 10231), Fusarium solani (ATCC
36031) and Acanthamoeba polyphaga (Ros), the latter
isolated from a case of Acanthamoeba keratitis which
occurred in the United Kingdom. The bacteria and fungi
were cultured according to recommended protocols for
contact lens disinfectant efficacy testing [8]. The F. solani
conidia were prepared as described previously [6]. A.
polyphaga (Ros) trophozoites were maintained in axenic
culture as described previously [7]. Cysts were produced
from the trophozoite cultures using Neff’s constant pH
encystment medium as described previously [7].
2.2. Test solutions
The PI contact lens disinfectant system (Clencide) was
supplied from the manufacturer (Ophtecs Corporation,
Osaka, Japan). The system comprises a sachet of disin-
fectant/proteolytic enzyme containing the PI (0.05 mg) and
Bacillus subtilis protease (8 mg), a neutralisation tablet
(sodium sulfite 2.4 mg) and a diluting/rinsing solution
(sodium borate, sodium chloride and EDTA). The dilut-
ing/rinsing solution (8 ml) is added to the contact lens storage
case and the disinfectant/proteolytic enzyme granules and
neutralising tablet added. The lenses are then placed inside
the case. The disinfection and neutralisation process is
complete within 10 min (a colour indicator in the system
Table 1
Efficacy of povidone iodine system against bacteria, fungi and Acanthamoeba p
Time P. aeruginosa
(ATCC 9027)
S. marcescens
(NCTC 10211)
S. aureus
(ATCC 6538)
C
(A
Log organism kill
0 0.0 0.0 0.0 0
5 min 5.6 (0.4)a 5.8 (0.3) 6.0 (0.1) 4
1 h –b – - –
2 h – – - –
3 h – – - –
4 h – – - –
a Mean (n = 3) log reduction in viable organisms with standard error of the mb No viable organism detect at this time point.
changes from orange to clear to show that the disinfection
stage is complete) but the lenses are left in the solution for at
least 4 h to effect the enzymatic cleaning. The lenses are then
removed from the case and rinsed with the remaining
diluting/rinsing solution before wearing.
The one-step hydrogen peroxide contact lens disinfectant
(AoSept, Ciba Vision, Atlanta, USA) was obtained locally
and comprises a 3% (v/v) hydrogen peroxide solution and a
contact lens storage case containing a platinum coated
neutralising disk. As with the PI system, the disinfection and
neutralisation process occurs simultaneously and the lenses
can be worn after 6 h.
Phosphate buffered saline (PBS) was used in place of the
disinfectant solutions in control studies. Dey–Engley Neutra-
lising Broth (Difco, MI, USA) was used in the PI studies and
0.02% (w/v) bovine liver catalase (Sigma Chemical
Company, Dorset, UK) for the hydrogen peroxide system.
2.3. Test methods
The systems were used exactly according to the
manufacturers’ recommendations and challenged with the
test organisms in a volume �0.1% of the disinfectant
solution volume. The challenge test assays for the bacteria
and fungi were conducted exactly in accordance with
recommended procedures [8].
The method for the Acanthamoeba trophozoites and cysts
was as described previously [7]. Sample time-points for the
PI system were after 0, 5 min and 1, 2, 3, 4 h exposure with
PI, and 0, 0.5, 1, 2, 4 and 6 h with the hydrogen peroxide
system. Experiments were conducted in triplicate.
In one experiment, the PI system was activated and left for
10 min before being challenged with P. aeruginosa. Viable
bacterial counts were then conducted over a 4-h period.
3. Results
3.1. PI disinfection system
Activity of the PI system against the test organisms is
shown in Table 1. Complete kill (5–6 log reduction)
olyphaga
. albicans
TCC 10231)
F. solani
(ATCC 36031)
A. polyphaga (Ros)
Trophozoites Cysts
.0 0.0 0.0 0.0
.7 (0.2) 4.8 (0.4) 4.5 (0.4) 1.0 (0.25)
– – 1.0 (0.3)
– – 2.8 (0.4)
– – 3.5 (0.3)
– – 3. 6 (0.2)
ean in parenthesis.
S. Kilvington / Contact Lens & Anterior Eye 27 (2004) 209–212 211
occurred with all bacteria and fungi tested by the first time
point of 5 min. With A. polyphaga, complete kill (4.5 log) of
trophozoites occurred within 5 min. For the cysts, a 2.8 log
reduction occurred after 2 h and 3.6 log by 4 h.
In the experiment where the system was challenged with
P. aeruginosa following a delay of 10 min after combining
the PI disinfectant, enzyme granules and neutralisation
tablet, no killing of the bacterium was detected over a 4-h
period; indicating that the disinfectant capacity of the system
is fully neutralised within 10 min.
No loss in organism viability was found in control studies
in which the test organisms were inoculated into PBS or the
Dey–Engley Neutralising Broth (results not shown).
3.2. One-step peroxide system
The efficacy of the hydrogen peroxide system against the
bacteria, fungi and A. polyphaga is shown in Table 2. The
system gave a 6 log kill of P. aeruginosa and S. marcescens
by 0.5 h (total kill for these bacteria) and a 4 log kill of S.
aureus at 1 h. With C. albicans, a 1 log kill was obtained
after 0.5 h, 2 log by 1 h and 5 log at 6 h. For F. solani conidia
only a 1.8 log kill was obtained by 6 h. A. polyphaga
trophozoites were reduced by 3.6 log (total kill) at 1 h but
only a 1.2 log reduction in cyst viability was found at 6 h.
Again, no change in organism viability was found in
control studies in which the test organisms were inoculated
into PBS or catalase neutraliser (results not shown).
4. Discussion
The suitability of contact lens disinfectant systems for
human use is determined by the Food and Drug Admin-
istration (FDA) and the International Organization for
Standardization [18]. In the ‘‘Stand Alone Test’’ (ISO
14729) employed here, a disinfectant must be capable of
reducing the viability of specified bacterial and fungal
species by 3 log (99.9%) and 1 log (90%), respectively
within the disinfection time recommended by the product
manufacturer [8]. However, there is no requirement to
demonstrate activity against Acanthamoeba [8].
Table 2
Efficacy of one-step hydrogen peroxide system against bacteria, fungi and Acan
Time P. aeruginosa
(ATCC 9027)
S. marcescens
(NCTC 10211)
S. aureus
(ATCC 6538)
C
(A
Log organism kill
0 0 0 0 0
0.5 h 6.4 (0.2)a 5.9 (0.3) 2.8 (0.3) 1.
1 h –b – 4.4 (0.2) 1.
2 h – – 4.7 (0.2) 2.
4 h – – – 2.
6 h – – – 5.
a Mean (n = 3) log reduction in viable organisms with standard error of the mb No viable organism detect at this time point.
In this study, we compared the disinfectant efficacy of a
novel PI contact lens disinfectant system with that of a one-
step hydrogen peroxide method. Although both products
surpassed the requirements of the ‘‘Stand Alone Test’’ for
bacteria and fungi, the PI system showed greater efficacy in
the rate of disinfection and activity against Acanthamoeba
cysts.
In the PI system the disinfectant is mixed with the proteo-
lytic cleaning granules in the lens storage case. A neutralising
tablet is added. Although the manufacturer recommends a 4-h
contact time, this is to enable the proteolytic cleaner towork; it
was found that the disinfectant stage is complete within
10 min. Under these conditions, the PI system produced at
least a 5 log reduction in bacteria and 4 log reduction in fungi
by the first sample point of 5 min. The system also
demonstrated good activity against Acanthamoeba, giving
a 4.5 log trophozoite kill by 5 min and a 2.8 or 3.6 log kill of
cysts within 2 and 4 h, respectively. It is not clear why killing
of the cysts continues, even after PI neutralisation is complete.
Possibly, the cysts take up the PI during the disinfection
process with lethal effect on the trophozoite within and that
this process continues progressively after the external
disinfectant has been neutralised. The efficacy of PI against
Acanthamoeba spp. has been reported elsewhere and is
confirmed by the findings of this study [4].
The one-step hydrogen peroxide system studied here
employs a platinum coated disc as part of the storage case
lens basket, to catalyse the breakdown of the disinfectant
into water and oxygen. Such a process offers the
convenience of a single disinfection-neutralisation step
and eliminates the painful consequence of inserting non-
neutralised lenses into the eye that can occur with two-step
systems. However, as has been previously described, the
rapid neutralisation of the peroxide results in decreased
efficacy against Acanthamoeba cysts in comparison with a
two-step system [7]. The system was also found to be less
effective than PI against fungi, giving only a 1.2 log and 1.8
log kill of F. solani conidia after 4 and 6 h exposure.
In conclusion, the PI system represents a new and
effective contact lens disinfectant system efficacious against
ocular pathogenic bacteria, fungi and Acanthamoeba.
However, unlike multipurpose disinfectant systems, once
thamoeba polyphaga
. albicans
TCC 10231)
F. solani
(ATCC 36031)
A. polyphaga (Ros)
Trophozoites Cysts
0 0 0
4 (0.2) 0 2.8 (0.3) 0
9 (0.4) 0.7 (0.2) 3.6 (0.1) 0.9 (0.3)
1 (0.4) 0.95 (0.1) – 0.9 (0.4)
5 (0.2) 1.2 (0.3) – 0.7 (0.3)
5 (0.4) 1.8 (0.2) – 1.2 (0.25)
ean in parenthesis.
S. Kilvington / Contact Lens & Anterior Eye 27 (2004) 209–212212
neutralisation is complete there is no residual disinfectant
activity for continued antimicrobial protection against
organisms that may have survived the disinfection process
or been introduced from the environment on opening the
storage case [20]. Accordingly, lenses should be re-
disinfected before wearing if they have been stored for
more than 24 h when using the PI system.
Acknowledgements
The technical assistance of Reanne Hughes and James
Lonnen is gratefully acknowledged. This study was
supported, in part, by a donation from Ophtecs Euro Ltd.,
Limerick, Ireland.
References
[1] Bourcier T, Thomas F, Borderie V, et al. Bacterial keratitis: predis-
posing factors, clinical and microbiological review of 300 cases. Br J
Ophthalmol 2003;87:834–8.
[2] Cheng KH, Leung SL, Hoekman HW, et al. Incidence of contact-lens-
associated microbial keratitis and its related morbidity. Lancet
1999;354:181–5.
[3] Dart JK, Stapleton F, Minassian D. Contact lenses and other risk
factors in microbial keratitis. Lancet 1991;338:650–3.
[4] Gatti S, Cevini C, Bruno A, et al. In vitro effectiveness of povidone-
iodine on Acanthamoeba isolates from human cornea. Antimicrob
Agents Chemother 1998;42:2232–4.
[5] Gorlin AI, Gabriel MM, Wilson LA, et al. Binding of Acanthamoeba
to hydrogel contact lenses. Curr Eye Res 1996;15:151–5.
[6] Hughes R, Dart J, Kilvington S. Activity of the amidoamine myr-
istamidopropyl dimethylamine against keratitis pathogens. J Antimi-
crob Chemother 2003;51:1415–8.
[7] Hughes R, Kilvington S. Comparison of hydrogen peroxide contact
lens disinfection systems and solutions against Acanthamoeba poly-
phaga. Antimicrob Agents Chemother 2001;45:2038–43.
[8] International Organization for Standardization: ISO 14729. Ophthal-
mic optics–contact lens care products–microbiological requirements
and test methods for products and regimens for hygienic management
of contact lenses. 2001.
[9] John T, Desai D, Sahm D. Adherence of Acanthamoeba castellanii
cysts and trophozoites to unworn soft contact lenses. Am J Ophthalmol
1989;108:658–64.
[10] Kilvington S, Larkin DF, White DG, et al. Laboratory investigation of
Acanthamoeba keratitis. J Clin Microbiol 1990;28:2722–5.
[11] Kilvington S, Larkin DFP. Acanthamoeba adherence to contact lenses
and removal by cleaning agents. Eye 1990;4:589–93.
[12] Lam DS, Houang E, Fan DS, et al. Incidence and risk factors for
microbial keratitis in Hong Kong: comparison with Europe and North
America. Eye 2002;16:608–18.
[13] Larkin DF, Kilvington S, Easty DL. Contamination of contact lens
storage cases by Acanthamoeba and bacteria. Br J Ophthalmol
1990;74:133–5.
[14] McLaughlin-Borlace L, Stapleton F, Matheson M, et al. Bacterial
biofilm on contact lenses and lens storage cases in wearers with
microbial keratitis. J Appl Microbiol 1998;84:827–38.
[15] Miller MJ, Ahearn DG. Adherence of Pseudomonas aeruginosa to
hydrophilic contact lenses and other substrata. J Clin Microbiol
1987;25:1392–7.
[16] Miller MJ, Wilson LA, Ahearn DG. Effects of protein, mucin, and
human tears on adherence of Pseudomonas aeruginosa to hydrophilic
contact lenses. J Clin Microbiol 1988;26:513–7.
[17] Morlet N, Duguid G, Radford C, et al. Incidence of Acanthamoeba
keratitis associated with contact lens wear. Lancet 1997;350:
414–6.
[18] Radford CF, Lehmann OJ, Dart JK. National Acanthamoeba Keratitis
Study Group. Acanthamoeba keratitis: multicentre survey in England
1992–6. Br J Ophthalmol 1998;82:1387–92.
[19] Radford CF, Minassian DC, Dart JK. Acanthamoeba keratitis in
England and Wales: incidence, outcome, and risk factors. Br J
Ophthalmol 2002;86:536–42.
[20] Rosenthal RA, Stein JM, McAnally CL, et al. A comparative study of
the microbiologic effectiveness of chemical disinfectants and perox-
ide-neutralizer systems. CLAO J 1995;21:99–110.
[21] Seal DV, Beattie TK, Tomlinson A, et al. Acanthamoeba keratitis. Br J
Ophthalmol 2003;87:516–7.
[22] Stapleton F, Dart JK, Seal DV, et al. Epidemiology of Pseudomonas
aeruginosa keratitis in contact lens wearers. Epidemiol Infect
1995;114:395–402.
[23] Stehr-Green JK, Bailey TM, Brandt FH, et al. Acanthamoeba keratitis
in soft contact lens wearers. A case-control study. J Am Med Assoc
1987;258:57–60.
Clinical Evaluation of OPL78 a Povidone-Iodine
Disinfection System with Silicone Hydrogel Lenses
Kiichi Ueda1), Masarnaru Inaba2), Yuko Miyamoto3), Yasutaka Kubota4), Naoki lwasaki4), Katsuhide
Yamasaki5) and Fumio Saitoh5) 1) Ueda Eye Clinic, 2) Inaba Eye Clinic, 3) Ai-ai Eye Clinic, 4) IWASAKI EYE CLINIC, 5) Ophtecs Corporation
Clinical Evaluation of OPL78 a Povidone-Iodine
Disinfection System with Silicone Hydrogel Lenses
Kiichi Ueda1), Masarnaru Inaba2), Yuko Miyamoto3), Yasutaka Kubota4), Naoki lwasaki4), Katsuhide
Yamasaki5) and Fumio Saitoh5) 1) Ueda Eye Clinic, 2) Inaba Eye Clinic, 3) Ai-ai Eye Clinic, 4) IWASAKI EYE CLINIC, 5) Ophtecs Corporation
OPL78, a chemical disinfection system for soft contact lenses that contains povidone-iodine as
the active ingredient, was clinically evaluated with silicone hydrogel lenses (SHCL). The study
included 65 patients (49 females, 16 males: mean age: 33±9.8 years). who used OPL78 to disinfect
a 2 weeks frequent replacement SHCL (or 12 weeks. then rated the usefulness of OPL78. We
conducted slit-lamp examination, observation of SHCL worn on eyes and microbiological
examination after patients had completed a disinfecting procedure. Finally. we conducted a
questionnaire survey. Anterior eye findings by slit-lamp examination did not change much during
the clinical evaluation. Though scratches and deposits were found on SHCL in some cases, these
did affect the wearing of the SHCL. The microbiological examination disclosed no problems.
Furthermore, the questionnaire Survey showed that the majority of respondents experienced no
problems while using OPL78 with SHCL. On the basis of these results, it is concluded that OPL78
is useful for disinfecting SHCL.
[Atarashii Ganka (Journa1 of the Eye) 27(9): 1310-1317. 2010]
Key words: OPL78. povidone-iodine, disinfection, silicone hydrogel, clinical evaluation
Introduction
Among the eye disorders caused by contact lenses (CLs), the most significant is corneal infection.
Recently, the incidence of corneal infections has been increasing, especially in users of 2-week
frequent-replacement soft contact lenses (SCLs), leading to a growing interest in disinfection of
SCLs.1,2) The chemical disinfectants currently used for SCLs include a multi-purpose solution (MPS)
system consisting of a single solution of polidronium chloride or polyhexamethylene biguanide
(PHMB) as the active ingredient and disinfectant systems that contain hydrogen peroxide or
povidone-iodine as the active ingredient. Most SCL users use an MPS, which is less effective than
other types of SCL disinfectants.3) Hydrogen peroxide-type disinfectants can cause
cytotoxicity-associated ocular disorders if hydrogen peroxide neutralization is insufficient. The
povidone-iodine-type disinfectant system has a broad antibacterial spectrum, is effective against fungi,
viruses, and amebae, and has been reported to have high corneal safety.4-11)
The use of 2-week frequent-replacement SCLs and one-day disposable SCLs has increased in recent
years, along with a rapid increase in the use of silicone hydrogel as a CL material.
While the conventional povidone-iodine type system consists of disinfection granules,
neutralization tablets, and a dissolution/rinse solution, the recently developed OPL78 system consists
of only disinfection granules and the neutralization tablet combined into a single tablet. We conducted
a clinical study to evaluate the efficacy of OPL78 as a disinfectant for 2-week frequent-replacement
silicone hydrogel contact lenses (SHCLs).
I. Subjects and Methods
1. Subjects
Sixty-five individuals were enrolled in the study from January 26, 2009, through June 30, 2009,
after receiving an explanation about the purpose and content of the study. Informed written consent
was obtained from all subjects prior to the study. The subjects consisted of 16 men and 49 women with
a mean age of 33.0 ± 9.8 years. The subject characteristics are shown in Figure 1.
Figure 1. Subject characteristics
*SCL: soft contact lens; **MPS: multi-purpose solution
2. Methods
a. Contact Lenses and Chemical Disinfectants
The subjects used four different 2-week frequent-replacement SHCL products. The ACUVUE®
OASYS™ product was studied in 20 subjects with 40 eyes. The AIR OPTIX® product was studied in
15 subjects with 30 eyes. The Medalist® Premier product was studied in 15 subjects with 30 eyes. The
2week Menicon PremiO product was studied in 15 subjects with 30 eyes. The specifications of the
evaluated SHCLs are shown in Table 1. In general, each SHCL was replaced every two weeks.
Subjects were instructed to wash their hands before handling the SHCLs.
Conventional
SCL* 1% Never used 1% One-day disposable
SCL* 11%
1-month
replacement SCL*
10%
2-week
frequent-replacement
SCL* 77%
MPS**
80%
(N = 65)
Type of Contact Lens Used Type of Disinfectant Used
Not answered
6% Never used 5%
Hydrogen
peroxide
disinfectant 9%
(N = 65)
Table 1. Lens specifications
Lens Name ACUVUE®
OASYS™
AIR
OPTIX®
Medalist®
Premier
2week Menicon
PremiO
Manufacturer Johnson & Johnson CIBAVision Bausch & Lomb Menicon
Polymer Senofilcon A Lotrafilcon B Balafilcon A Asmofilcon A
Dk/L * 147 138 101 161
Moisture content (%) 38 33 36 40
Base curve (mm) 8.4 8.6 8.6 8.3, 8.6
Replacement Schedule 2 weeks, daily wear 2 weeks, daily wear
2 weeks, daily wear/
6 consecutive nights,
continuous wear
2 weeks, daily wear
* Oxygen transmission rate = * 10-9 (cm/s) * (mL O2/[mL∙mmHg])
The constituents of the OPL78 povidone-iodine disinfectant system are shown in Figure 2. Proper
usage of the OPL78 system is illustrated in Figure 3. In the OPL78 system, the active disinfectant and
the neutralization/cleaning component have been combined into a single tablet, designated OPL78-I,
which is dissolved in the dissolution/rinse solution, designated OPL78-II, before use. Although
scrubbing is not required for lens cleaning according to the directions provided with the OPL78
system, subjects whose lenses had greater amounts of deposits were instructed to scrub their SHCLs
with the OPL78-II dissolution/rinse solution.
Figure 2. Constituents of OPL78
OPL78-I (press-coated tablets) Outer layer:
• povidone-iodine (disinfectant)
Inner layer:
• sodium sulfite (neutralizer)
• proteolytic enzyme (cleaning agent)
OPL78-II (dissolution/rinse solution)
• sodium chloride, boric acid
Disinfectant Lens case
Lens case Neutralizer/cleaning agent
Figure 3. Usage of OPL78
b. Observation time-points and assessments
Subjects used the OPL78 system to disinfect their SHCLs for 12 weeks. Assessments performed in
this study included slit-lamp microscopy for the anterior eye, inspection of the lens condition after use,
microbiological examination, and a questionnaire survey (Table 2). The slit-lamp microscopy findings
for the anterior eye and the subjective symptoms recorded in the questionnaire were scored according
to the criteria shown in Table 3. After use, the lenses were inspected for deposits and scratches using a
slit-lamp microscope. Twelve weeks after the start of the study, the subjects responded to a
questionnaire regarding the usability of the OPL78 system (i.e., to what extent using the OPL78
system felt convenient), the cleaning ability of the OPL78 system (to what extent OPL78 appeared to
remove deposits from the SHCL), and the comfortableness of the SHCLs (to what extent wearing the
SHCL that was disinfected with OPL78 felt comfortable). The SHCLs were collected from the
subjects 2 weeks after initiation of the study and microbiologically evaluated according to the
procedure, methods, and criteria12) defined in Table 4. The presence of Staphylococcus aureus,
Pseudomonas aeruginosa, Escherichia coli, and Serratia spp., which are often regarded as clinically
relevant in ophthalmology, was evaluated and the OPL78 system was considered to have no efficacy if
Put OPL78-I and OPL78-II into the case with the lens.
Orange color during disinfection Colorless after completion
Allow to stand for at least 4 h.
Shake horizontally
Wear the lens
Replace the solution in the case with OPL78-II and rinse the lens.
Color disappears
at least one of these bacteria was detected. Bacteria detected only following an enrichment culture
were considered not present (negative result)12).
Table 2. Characteristics of each assessment
Assessment Content Baseline After
2 weeks
After
4 weeks
After
8 weeks
After
12 weeks
Anterior eye
findings
Staining of the corneal epithelium, SEALs*,
corneal edema, corneal infiltrate, corneal
ulcer, neovascularization, conjunctival
injection, and papillary hyperplasia
Lens condition
after use
Scratches, deposits, deformation, and
discoloration
Microbiological
examination See Table 4
Questionnaire Foreign body sensation, dryness, itching,
fogginess, and other items **
* SEALs: superior epithelial arcuate lesions
** At week 12, the questionnaire also assessed each subject’s overall impression of the OPL78 system.
Table 3. Scoring criteria for anterior eye findings and subjective symptoms
1) Criteria for anterior eye findings
A) Corneal findings
Corneal staining
(Extent) (Density)
0: No staining 0: No staining
1: 1–25% of the corneal surface 1: Low density
2: 26–50% of the corneal surface 2: Moderate density
3: 51–75% of the corneal surface 3: High density
4: 76–100% of the corneal surface
SEALs Cell infiltration/ulcer of the corneal stroma
0: None 0: None
1: Mild 1: Cell infiltration
2: Moderate 2: Ulcer
3: Severe
Corneal edema Corneal neovascularization
0: None 0: None
1: Epithelial edema 1: Less than 2 mm from the corneal limbus
2: Stromal edema (including Descemet membrane folds) 2: 2 mm or more from the corneal limbus
3: Total edema of the cornea 3: 2 mm or more from the corneal limbus in
multiple directions or stromal
neovascularization
B) Conjunctival findings
Conjunctival injection Papillary hyperplasia of the upper eyelid
0: None 0: None
1: Less than 1/2 1: Only the forniceal conjunctiva
2: 1/2 or more 2: The forniceal conjunctiva + less than 1/2 of
the tarsal conjunctiva
3: Entire perimeter 3: The forniceal conjunctiva + 1/2 or more of
the tarsal conjunctiva
Others
0: None
1: Mild
2: Moderate
3: Severe
2) For subjective symptoms
0: None
(Feel no annoying symptoms)
1 Mild
(Occasionally feel a symptom, but almost always feel
good)
2: Moderate
(Always feel a symptom, but no need for temporary
discontinuation of use)
3: Severe
(Always feels strong symptoms and cannot wear the lens)
Table 4. Procedure, methods, and criteria for the microbiological examination
Procedure
[1] After care with the OPL78 system, collect the CL in the
lens case
[2] Put each CL into a sterilized PP tube filled with 2 mL
DPBS
[3] Agitate the tube with a vortex mixer for 1 minute [4] After agitation, culture both CL and solution
Culturing Methods
[1] Trypticase soy agar with 5% sheep blood 35 °C, 24–48 h
[2] Chocolate II agar 37 °C, 5% CO2, 24–48 h
[3] Thioglycollate broth 37 °C, 7 days with enrichment medium
[4] Soybean-casein digest agar 37 °C, 5 days with enrichment medium (with CL buried)
For [1] and [2], 200 μL of the solution was used after agitation. For [3], all of the solution was used after agitation.
Examination Criteria12)
Culture result of the CL after disinfection with the
OPL78 system
Specific bacteria* Total bacterial count (cfu/mL)
Highly Effective Not detected 0–<103
Effective Not detected 103–<105
Not Effective Detected 105 or more
* Specific bacteria: S. aureus, P. aeruginosa, E. coli, Serratia spp.
c. Statistical Method
Scores for the anterior eye findings and subjective symptoms at week 12 were compared with those
at the study initiation using the Wilcoxon signed rank test with a significance level of 0.05.
II. Results
1. Anterior Eye Findings
At the initiation of the study, staining of the corneal epithelium, corneal neovascularization,
conjunctival injection, papillary hyperplasia of the upper eyelid, pigmented slide, dimple veiling, and
corneal scarring were seen in some patients, but all cases were mild in severity, so all subjects
continued the study. The severity of these findings at week 12 was not different from the baseline
severity. During the study, superior epithelial arcuate lesions (SEALs) and conjunctival injection were
found in one eye and two eyes, respectively, and all cases were mild (Table 5).
Table 5. Anterior eye findings
Symptom Severity *1 Time Point
p-value *2
Corneal
staining-extent
0 105 eyes 97 eyes 94 eyes 104 eyes 103 eyes
0.9094 1 22 27 36 26 25
2 3 6 0 0 2
3 3 0 0 0 0
Corneal
staining-density
0 105 97 94 104 103
0.8832 1 22 32 32 22 25
2 3 1 4 4 2
3 0 0 0 0 0
SEALs
0 130 129 130 130 129
- 1 0 1 0 0 1
2 0 0 0 0 0
3 0 0 0 0 0
Corneal
infiltration/ulcer
0 130 130 130 130 130
- 1 0 0 0 0 0
2 0 0 0 0 0
3 0 0 0 0 0
Corneal edema
0 130 130 130 130 130
- 1 0 0 0 0 0
2 0 0 0 0 0
3 0 0 0 0 0
Corneal
neovascularization
0 126 128 128 128 128
0.1797 1 1 3 1 1 1
2 2 1 1 1 1
3 0 0 0 0 0
Conjunctival
injection
0 130 130 129 130 130
- 1 0 0 0 0 0
2 0 0 0 0 0
3 0 0 0 0 0
Papillary
hyperplasia of the
upper eyelid
0 126 126 127 126 128
0.1797 1 4 4 2 4 2
2 0 0 0 0 0
3 0 0 0 0 0
Others *3
0 124 124 124 123 124
- 1 6 6 6 7 6
2 0 0 0 0 0
3 0 0 0 0 0
*1: See Table 3 for scoring criteria.
*2: The Wilcoxon signed rank test was used to compare scores at the study initiation and at week 12. -: Statistical test could
not be carried out because the scores at the study initiation and at week 12 were both 0 or there were very few subjects.
*3: Other findings included pigmented slide, dimple veiling, and corneal scarring.
2. Lens Condition after Use
Deposits were found on the SHCLs for 22 eyes (16.9%) at the end of week 2, but found for only 9
eyes (6.9%) at week 12. Among the subjects for whom deposits were found on the SHCL after use, 4,
7, and 4 subjects were instructed to scrub the SHCLs at week 2, 4, and 8, respectively, because the
deposit level was regarded as high. Scratches were found on the SHCL for 2–7 eyes (1.5%–5.4%) at
week 2 and later, but all cases were mild, allowing all subjects to continue to use the SHCL. Metals
and lacquer were each found on the SHCL for one eye (Figure 4). No deformation abnormalities were
found during the study period.
Figure 4. Lens condition after use
3. Microbiological examination
Specific bacteria (S. aureus, P. aeruginosa, E. coli, and Serratia spp.) were not detected in any of
the 130 samples evaluated. The total bacterial count was 0–<103 cfu/mL for 128 samples and 103–<105
cfu/mL for 2 samples. Therefore, the OPL78 system was highly effective for 98.5% of the samples and
effective for 1.5% of the samples (Table 6). The bacteria detected in the two cases with bacterial
counts of 103–<105 cfu/mL were Staphylococcus and Corynebacterium.
Table 6. Microbiological examination
Total Bacterial Count
(cfu/ml)
Category
0–<103 103–<105 105 or more
n* 128 2 0
Specific Bacteria Not detected Not detected -
Effectiveness Highly effective Effective -
* Bacterium detected only with an enrichment culture were considered not present (negative result). (N = 130)
4. Questionnaire Survey
In the questionnaire to assess subjective symptoms, most of the subjects reported that they could
generally use the lenses comfortably. The most frequently reported subjective symptoms were a
feeling of dryness (20.8%–34.6% of eyes), foreign body sensation (3.9%–15.4%), and itching
(0.8%–11.5%). The incidence of itching at week 12 was significantly different from the incidence at
the start of the study (p = 0.0128), but no significant difference was observed for any other symptom
(Figure 5). Most subjects (77%–80%) answered “very good” or “good” when asked about the
comfortableness when wearing the lens, the cleaning ability of the OPL78 system, and the usability of
the OPL78 system, and 68% of subjects showed willingness to continue to use the OPL78 system
(Figure 6).
* Number of lenses for which abnormalities such as
deposit or scratch were found from a total of 130
lenses at each time point
Nu
mber
of
len
ses*
*
Deposits
Scratches
Others
Metals on the lens
Lacquer on the lens
Week 2 Week 4 Week 8 Week 12
Time Point
(Duplicated count was allowed.)
Figure 5. Questionnaire survey (subjective symptoms)
Figure 6. Questionnaire survey (overall evaluations)
Impression regarding use Willingness to continue use
Comfortableness when
wearing the lens
Cleaning ability of
OPL78
Usability of OPL78
Very Good
Good
Average
Bad
Very Bad
Not want to use
1%
May or may
not use
31%
Want to use
68%
(N of subjects = 65) (N of subjects = 65)
Feeling of Dryness Foreign-body sensation
Itching Fogginess
Num
ber
of
eyes
Initiation
Num
ber
of
eyes
Nu
mb
er o
f ey
es
Nu
mb
er o
f ey
es
Week 2 Week 4 Week 8 Week 12 Initiation Week 2 Week 4 Week 8 Week 12
Initiation Week 2 Week 4 Week 8 Week 12 Initiation Week 2 Week 4 Week 8 Week 12
Time Point Time Point
Time Point Time Point
(Total number of eyes = 130) (Total number of eyes = 130)
(Total number of eyes = 130) (Total number of eyes = 130)
Severity 0: None 1: Mild 2: Moderate 3: Severe
III Discussion
In this study, 65 subjects (130 eyes) were observed for 12 weeks to evaluate the clinical benefit of
the OPL78 system when it is used as a disinfectant system for SHCLs, which were introduced in
recent years.
In aqueous solution, povidone-iodine, the disinfectant component of the OPL78 system, releases
available iodine (I2 and I3-), which has high cell permeability and kills bacteria by oxidizing thiol
groups in membrane proteins, enzymes, and nuclear proteins. Because povidone-iodine has a broad
antibacterial spectrum, yet produces little skin irritation, it is widely utilized for various clinical
purposes, including disinfection of mucosal surfaces, fingers, and skin. Povidone-iodine has also been
developed as a chemical disinfectant for soft contact lenses and has been reported to have a high
disinfection efficacy against bacteria, fungi, Acanthamoeba, and viruses, with a high level of safety4,5).
In this clinical study, the four types of bacteria that are often regarded as clinically relevant, S. aureus,
P. aeruginosa, E. coli, and Serratia spp., were not detected in any of the samples from the 130 eyes.
The disinfectant system was determined to be highly effective for samples from 128 eyes and effective
for those from two eyes. The bacteria detected in the samples from the two effective cases were mostly
Staphylococcus and Corynebacterium, which were probably indigenous bacteria in the conjunctival
sac and skin. We isolated and cultured the detected Staphylococcus and Corynebacterium bacteria and
loaded the OPL78 disinfection solution with 105–106 cfu/mL of each type, and found that all bacteria
were killed. Although the microbiological examination was conducted by collecting the lens case with
the lens and the post-neutralization solution in it after lens care by the subject, bacteria attached on the
inside surface of the case that had not been exposed to the disinfection solution may have been
detected owing to incomplete filling of the solution into the case. Because of the results of the
microbiological examination, as well as the lack of symptoms or findings of suspected infection
during the study period, the OPL78 system was considered effective as a disinfectant for SHCLs.
The anterior ocular findings observed during the study period by slit-lamp microscopy were mild in
severity and known to be relatively common in SCL or SHCL users. Corneal staining can occur in
those who use SHCLs in combination with a multi-purpose solution containing PHMB13,14), because
the disinfectant component absorbed into the lens could affect corneal epithelial cells. In addition,
mechanical stimulation of the cornea by harder SHCLs is considered to have the possibility to affect
corneal epithelial cells 13). In this study, the extent and density of corneal staining did not change from
the start of study through week 12, because the disinfectant was less likely to remain in the lens due to
the disinfection process utilized with the OPL78 system, in which the disinfection component is
neutralized and the lens is rinsed before wearing.
Clenside®, the first povidone-iodine disinfectant product developed in Japan, could cause
delayed-onset drug allergy-like symptoms in some users of conventional SCLs15). The OPL78 system,
utilizing the same components for disinfection, neutralization, and cleaning as were used in Clenside®,
did not cause drug allergy-like symptoms in this study, in which subjects used SHCLs. Even if one
does not consider the materialistic difference between conventional SCLs and SHCLs, late-onset
allergic symptoms cannot be evaluated in a study of only 12 weeks, so caution should be exercised
during long-term use of the OPL78 system.
During the study period, hordeolum was reported as an adverse effect in one eye, but was not
considered a side effect of the OPL78 system, because the causal relationship with OPL78 use was
unclear.
Some deposits were identified during examination of the condition of the lenses after use of the
OPL78 system. Although the OPL78 system contains cleaning agents, including a protease, its
cleaning ability could be insufficient for SHCLs on which lipids are more likely to deposit, in which
case the user should be instructed to scrub the lens with the OPL78 dissolution/rinse solution. It was
unclear why deposits were more likely to be observed at week 2 than at the other time points; however,
a possible explanation for this finding is that eye secretions increased until the subjects were
accustomed to the lens, because many of the subjects used SHCLs for the first time in this study.
The most common subjective symptoms reported in the questionnaire, in order of decreasing
incidence, were a feeling of dryness, foreign body sensation, and itching. Although the severity of
itching at week 12 was significantly different from the severity at baseline, most subjective symptoms
were mild and no discontinuation of contact lens use occurred. The observed subjective symptoms
were consistent with those described in clinical reports on other SHCLs. In a clinical study by Shinoda
et al., in which subjects used a one-month replacement SHCL together with a hydrogen peroxide
disinfectant for three months, the subjective symptoms reported in the three month observation period
and their incidences were similar to those reported in the present study; the most common subjective
symptoms were dryness (incidence: 10.3%–33.3%), foreign body sensation (10.3%–20.5%), and
itching (5.1%–7.7%)16). Moreover, the foreign body sensation reported in the present study may be due
to deposits on the SHCLs and the mechanical stimulation of the SHCL mentioned above.
Contact lens users are required to strictly adhere to defined lens care procedures. There exists a need
for a new povidone-iodine system that can be used with a simpler disinfection procedure than the
conventional method that requires adding three agents4). To use the OPL78 system, one only needs to
dissolve OPL78-I into OPL78-II. The questionnaire survey in this study showed that 77% of subjects
responded that the usability of OPL78 was very good or good, while 80% of subjects responded that
the cleaning ability of OPL78 and comfortableness when wearing the lens were very good or good. As
a result, 68% of subjects showed willingness to continue using the OPL78 system, resulting in a good
overall rating for the system.
The results of this study demonstrate that the OPL78 system is safe, highly effective, and easy to
use. Therefore, the OPL78 system is an ideal disinfectant system for SHCLs with advantages over
currently available disinfectant systems.
文献
Comparison of the Antibacterial and Antifungal Effects of a
Contact Lens Solution Containing Povidone-Iodine and Three
Other Solutions
Ryoji Yanai
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Department of Ophthalmology, Toyota Chuo Hospital
Kiichi Ueda
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Shimonoseki City (Ueda Eye Clinic)
Motoharu Tajiri, Toru Matsumoto, Shigeru Nakamura and Fumio Saito
Ophtecs Corporation Research Center
Teruo Nishida
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine
Comparison of the Antibacterial and Antifungal Effects of a
Contact Lens Solution Containing Povidone-Iodine and Three
Other Solutions Ryoji Yanai
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Department of Ophthalmology, Toyota Chuo Hospital
Kiichi Ueda
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Shimonoseki City (Ueda Eye Clinic)
Motoharu Tajiri, Toru Matsumoto, Shigeru Nakamura and Fumio Saito
Ophtecs Corporation Research Center
Teruo Nishida
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine
We compared the disinfectant effects of a solution for soft contact lens care that contained povidone
iodine (PVP-I) with the effects of 3 other solutions for contact lens care, specifically solutions that
contained hydrogen peroxide, polydronium, or polyhexanide as the active ingredient against bacteria
and fungi. All disinfectant solutions demonstrated antibacterial activity against Pseudomonas
aeruginosa, Staphylococcus aureus, and Serratia marcescens, and antifungal activity against
Fusarium solani within the time recommended for disinfection using commercially available
solutions. However, only the solution containing PVP-I was effective against Candida albicans. These
results suggest that contact lens solutions that contain PVP-I are useful as disinfectant solutions for
soft contact lenses.
(J Jpn CL Soc 47: 32-36, 2005)
Key Words : Povidone-Iodine(PVP-Ⅰ), Chemical Disinfection, Lens Care, Antibacterial Activity, Antifungal Activity
Introduction
Soft contact lenses (SCLs), which have high moisture contents, are susceptible to attachment by
pathogenic microorganisms, often resulting in serious CL-related eye disorders such as corneal ulcers.
Thus, the use of SCLs requires regular disinfection of the lenses to remove microorganisms. The
methods for SCL disinfection are roughly classified into 2 types: heat disinfection (boiling
disinfection) and cold disinfection (chemical disinfection). Boiling disinfection methods were initially
developed and widely used by SCL wearers. However, chemical disinfection was subsequently
developed to overcome various problems including allergies to proteins denatured by heating,
deterioration of SCLs, and failure or malfunction of the boiling apparatus. In Japan, solutions
containing hydrogen peroxide as the active ingredient and multipurpose solutions, second- and
third-generation chemical disinfectants, respectively, were introduced and spread rapidly in the 1990s.
However, chemical disinfectants are not effective against a large number of bacterial cells or fungi
such as Candida and are thus considered to have a weaker disinfectant effect than boiling1).
Iodine-based disinfectants, which contain povidone-iodine (PVP-I), a halogen compound
synthesized by Gershenfeld in 1957, exert a bactericidal effect via iodine (I2) release. They are
effective against a wide range of microorganisms including vegetative bacteria, spores, tubercle
baccilli, viruses, and fungi2)-7). In addition, they cause less skin irritation as compared to alcohol and
are nearly odorless. For these reasons, they are currently the most commonly used medical
disinfectants for hand, surgical skin, and mucosal disinfection8)-10). Chemical disinfectants containing
PVP-I as the active ingredient have recently been commercialized in Japan, and have the following 3
properties: a broad microbial spectrum, an immediate disinfectant effect, and safety with respect to the
body.
In this study, we compared the antibacterial and antifungal effects of a chemical disinfectant
containing PVP-I as the active ingredient with those of conventional disinfectants that contain
hydrogen peroxide, polidronium chloride, or polyhexanide chloride.
Methods
1. Test Solutions
A PVP-I-based disinfectant product (Ophtecs, Kobe, Japan), a hydrogen peroxide-based disinfectant
product (Abbott Medical Optics Japan, Tokyo, Japan), a polidronium chloride-based disinfectant
product (Alcon Japan, Tokyo, Japan), and a polyhexanide chloride-based disinfectant product (Abbott
Medical Optics Japan) were used as the test solutions.
Test strains were selected according to ISO 1472911). For bacteria, Pseudomonas aeruginosa
(13275; Institute for Fermentation Osaka [IFO], Japan), Staphylococcus aureus (13276, IFO), and
Serratia marcescens (13880; American Type Culture Collection [ATCC], USA) were used, all of
which are frequently reported as causative organisms for corneal infections related to CLs12),13). For
fungi, Fusarium solani (36031, ATCC) was selected as a representative filamentous fungi and
Candida albicans (1594, IFO) as a representative yeast species.
2. Methods for Inoculum Preparation
1) Bacteria
The test strain was cultured on soybean-casein digest agar slants at 35°C for 18 to 24 hours, and
then bacterial cells were harvested with Dulbecco's phosphate-buffered saline (DPBS).
2) Fungi
The F. solani test strain was cultured on potato dextrose agar plates at 25°C for 10 to 14 hours, and
then spores were harvested with DPBS. The C. albicans test strain was cultured on Sabouraud
dextrose agar slants at 25°C for 42 to 48 hours, and then bacterial cells were harvested with DPBS.
The cell suspension was filtered through absorbent cotton and centrifuged at 2,000 × g for 10 minutes
at 25°C. The resulting supernatant was discarded, and the precipitate was suspended in DPBS. The
turbidity of the suspension was measured with a turbidimeter. The concentration of the suspension was
adjusted to 1.0 × 107 to 1.0 × 108 colony-forming units (cfu)/ml11).
3. Methods of Testing for Disinfectant Effects
The inoculum was added to each test solution at final concentrations ranging from 1.0 × 105 to 1.0 ×
106 cfu/ml and disinfected for a period of time corresponding to 25%, 50%, 75%, or 100% (1.25
minutes to 4 hours) of the recommended disinfection time for each test solution (Table 1). Disinfection
was performed according to the methods described in the package insert for each test solution. To stop
the disinfection reaction, the solution containing PVP-I was neutralized with 0.003% sodium sulfite
solution and the solution containing hydrogen peroxide with 0.01% catalase solution. The solutions
containing polidronium chloride or polyhexanide chloride were neutralized with Dey/Engley
neutralizing broth, although neutralization is not required for normal lens disinfection11). After
neutralization, bacteria were cultured by the pour plate method with soybean-casein digest agar at
35°C for 4 to 6 days and fungi with glucose peptone agar at 25°C for 5 to 6 days. Colonies were
counted to calculate the number of viable cells11).
Table 1 Recommended Disinfection Time for Each Chemical Disinfectant
Test Solution Disinfection Time
Povidone-iodine-based solution ≥ 5 minutes
Hydrogen peroxide-based solution ≥ 10 minutes
Polidronium chloride-based solution ≥ 4 hours
Polyhexanide chloride-based solution ≥ 4 hours
4. Evaluation of the Disinfectant Effect
The disinfectant effect of each test solution was evaluated according to the stand-alone test
described in ISO 1472911). A disinfectant effect was defined as a reduction in the number of cells to
less than 1/1000 the number of loaded cells for bacteria and to less than 1/10 for fungi11),14).
Results
1. Antibacterial Activity
The antibacterial activities of the various chemical disinfectants were compared using linear
regression. For P. aeruginosa, the number of the cells was reduced to below the detection limit within
the recommended disinfection time by all of the chemical disinfectants, and thus they demonstrated
effective antibacterial activity. In addition, the number of loaded cells was already reduced to less than
1/1000 in 25% of the recommended disinfection time, for all disinfectants. Specifically, effective
antibacterial activity was achieved in 1.25 minutes for the PVP-I solution group, in 2.5 minutes for the
hydrogen peroxide solution group, and in 1 hour for the polidronium chloride and polyhexanide
chloride solution groups (Fig. 1).
Fig. 1 Antibacterial activity against Pseudomonas aeruginosa
: Povidone-iodine solution group
: Hydrogen peroxide solution group
: Polidronium chloride solution group
: Polyhexanide chloride solution group
For Staphylococcus aureus, the number of loaded cells was reduced to below the detection limit
within the recommended disinfection time in the PVP-I, hydrogen peroxide, and polyhexanide
chloride solution groups, but not in the polidronium chloride solution group. In addition, the number
of loaded cells was reduced to less than 1/1000 in 25% of the recommended disinfection time for the
PVP-I and polidronium chloride solution groups, in 50% for the polyhexanide chloride solution group,
and in 75% for the hydrogen peroxide solution group. Therefore, effective antibacterial activity against
S. aureus was achieved in 1.25 minutes for the PVP-I solution group, in 7.5 minutes for the hydrogen
peroxide solution group, in 1 hour for the polidronium chloride solution group, and in 2 hours for the
polyhexanide chloride solution group (Fig. 2).
Fig. 2 Antibacterial activity against Staphylococcus aureus
: Povidone-iodine solution group
: Hydrogen peroxide solution group
: Polidronium chloride solution group
: Polyhexanide chloride solution group
For Serratia marcescens, similar to the results for Staphylococcus aureus described above, the
number of loaded cells was reduced to below the detection limit within the recommended disinfection
time in the PVP-I, hydrogen peroxide, and polyhexanide chloride solution groups, but not in the
polidronium chloride solution group. The number of loaded cells was reduced to below the detection
Num
ber
of
via
ble
mic
roorg
anis
ms
(log10)
Disinfection time Disinfection time
(Minute) (Hour)
Num
ber
of
via
ble
mic
roorg
anis
ms
(log10)
Disinfection time Disinfection time
(Minute) (Hour)
limit in 25% of the recommended disinfection time for the PVP-I and polyhexanide chloride solution
groups, in 50% for the hydrogen peroxide solution group, and in 75% for the polidronium chloride
solution group. Therefore, effective antibacterial activity on S. marcescens was achieved in 1.25
minutes for the PVP-I solution group, in 5 minutes for the hydrogen peroxide solution group, in 1 hour
for the polyhexanide chloride solution group, and in 3 hours for the polidronium chloride solution
group (Fig. 3).
Fig. 3 Antibacterial activity against Serratia marcescens
: Povidone-iodine solution group
: Hydrogen peroxide solution group
: Polidronium chloride solution group
: Polyhexanide chloride solution group
2. Antifungal Activity
For F. solani, the loaded cells were all sterilized and thus the cell number was reduced to below the
detection limit within the recommended disinfection time in the PVP-I, polidronium chloride, and
polyhexanide chloride solution groups. There was limited antifungal activity, with a reduction to up to
1/100 of the number of loaded cells, within the recommended disinfection time in the hydrogen
peroxide solution group. In addition, the number of loaded cells was reduced to less than 1/10 in 25%
of the recommended disinfection time for all disinfectants. Therefore, effective antifungal activity was
achieved in 1.25 minutes for the PVP-I solution group, in 2.5 minutes for the hydrogen peroxide
solution group, and in 1 hour for the polidronium chloride and polyhexanide chloride solution groups
(Fig. 4).
Num
ber
of
via
ble
mic
roorg
anis
ms
(log10)
Disinfection time Disinfection time
(Minute) (Hour)
Fig. 4 Antifungal activity against Fusarium solani
: Povidone-iodine solution group
: Hydrogen peroxide solution group
: Polidronium chloride solution group
: Polyhexanide chloride solution group
For C. albicans, sufficient antifungal activity was obtained for the PVP-I solution group; the
number of loaded cells was reduced to below the detection limit in 25% of the recommended
disinfection time. In contrast, the number of loaded cells was not reduced to less than 1/10 within the
recommended disinfection time and thus no effective antifungal activity was obtained in the hydrogen
peroxide, polidronium chloride, and polyhexanide chloride solution groups (Fig. 5).
Fig. 5 Antifungal activity against Candida albicans
: Povidone-iodine solution group
: Hydrogen peroxide solution group
: Polidronium chloride solution group
: Polyhexanide chloride solution group
Discussion
We compared the antibacterial and antifungal effects of a chemical disinfectant containing PVP-I as
the active ingredient with those of 3 conventional chemical disinfectants. The PVP-I solution reliably
exerted sufficient disinfectant effects against both bacteria and fungi more rapidly than the other
chemical disinfectants. In addition, the solutions containing hydrogen peroxide, polidronium chloride,
or polyhexanide chloride provided sufficient disinfectant effects against bacteria and F. solani, but
Num
ber
of
via
ble
mic
roorg
anis
ms
(log10)
Disinfection time Disinfection time
(Minute) (Hour)
Num
ber
of
via
ble
mic
roorg
anis
ms
(log10)
Disinfection time Disinfection time
(Minute) (Hour)
showed no antifungal effect against C. albicans within the study period (Table 2). Our study suggested
that PVP-I solutions have a higher disinfectant effect than conventional chemical disinfectants.
Table 2 Antibacterial and Antifungal Activities of the Chemical Disinfectants
Bacteria Fungi
PA SA SM FS CA
Povidone-iodine solution + + + + +
Hydrogen peroxide solution + + + + -
Polidronium chloride solution + + + + -
Polyhexanide chloride solution + + + + -
PA: Pseudomonas aeruginosa, SA: Staphylococcus aureus, SM: Serratia marcescens, FS: Fusarium solani, CA: Candida
albicans
All chemical disinfectants studied had sufficient antibacterial effects. However, the polidronium
chloride and polyhexanide chloride solutions required 1 hour or more, while the PVP-I solution was
effective within 1 minute; therefore, it was characterized as having an immediate disinfectant effect. In
addition, greater numbers of viable cells were observed for Staphylococcus aureus and Serratia
marcescens than for P. aeruginosa after disinfection with the polidronium chloride or polyhexanide
chloride solutions; therefore, these disinfectants were considered less likely to exert sufficient
antibacterial effects against the former 2 bacterial species. These results raise concerns regarding the
disinfectant effect of multipurpose solutions against a large number of bacteria, depending on the
strain. Furthermore, multipurpose solutions promote adhesion of P. aeruginosa to corneal epithelial
cells15) and thus potentially increase the risk of corneal infection. The PVP-I and hydrogen peroxide
solutions rapidly exhibited sufficient bactericidal effects and thus were considered excellent
disinfectants. However, since they exerted no disinfectant effect against microbial contamination after
neutralization, re-disinfection of SCLs is required when a lens case is opened accidentally after
disinfection, re-exposing SCLs to microorganisms. Multipurpose solutions do not typically require
neutralization and provide a long-lasting disinfectant effect once the disinfection reaction occurs. For
this reason, multipurpose solutions are considered suitable for long-term storage. In fact, polidronium
chloride solutions have shown antibacterial effects against P. aeruginosa and Staphylococcus aureus
even 3 days after disinfection16).
For fungi, all of the disinfectants studied showed effective antifungal activity against F. solani, but
only the PVP-I solution had a sufficient antifungal effect against C. albicans. The yeast C. albicans is
the most frequent causative organism for keratomycosis, and thus a high antifungal activity against the
species is an essential property of a chemical disinfectant. Based on the results of our study, C.
albicans is difficult to control with hydrogen peroxide or multipurpose solutions. Since C. albicans is
present in daily living spaces, there is a risk of SCLs contamination by fingers that are not fully
disinfected with hydrogen peroxide or multipurpose solutions. Results similar to those of our study
have been noted in a previous investigation by the National Consumer Affairs Center of Japan1). C.
albicans disinfection is a serious problem for SCL hygiene. With respect to the time required to
disinfect fungi, the PVP-I solution provided sufficient effects within 1 minute; therefore, it was
considered to have an immediate disinfectant effect against fungi.
PVP-I has disinfectant effects against a wide variety of microorganisms, such as viruses and
Acanthamoeba as well as bacteria and fungi17). We plan to investigate the disinfectant effects of PVP-I
solutions for a broader sample of microorganisms. In addition, since PVP-I solutions contain various
additives in addition to the disinfection component, further investigations are needed to determine
whether deterioration and deformation of SCLs could occur due to the reaction between such additives
and polymers including SCL materials and a lens case. Additionally, more studies are required
regarding the disinfectant effects of PVP-I solutions, for example, on the extent to which PVP-I can
exert a disinfectant effect against a biofilm formed inside a lens case. Finally, the compliance of SCL
users represents a very important issue. Compliance is worse for PVP-I solutions that require a total of
3 agents for SCL care than for single, multipurpose solutions that account for all procedures related to
SCL care. Thus, development of a simple procedure for disinfection is desired in terms of the
compliance of CL wearers.
文献
1) 「ソフトコンタクトレンズ」の衛生状態等について調べる─ソフトコンタクトレンズ用
消毒剤のテストも加えて─.国民生活センター02-12:11-17, 2003.
2) 安生紗枝子,加賀美操,佐藤たか子,大倉真知子他:病院で常用されている消毒薬のグ
ラム陰性桿菌感染症および opportunistic infectionの原因菌となる菌種に対する殺菌作用.
防菌防微 5: 204-208, 1977.
3) 加賀谷けい子,谷口啓子,深沢義村,西川武二:ポビドンヨードの病原性酵母に対する
殺菌効果.真菌誌 21: 286-292, 1980.
4) Rackur H:New aspects of mechanism of action of povidone-iodine. J Hospital Infect 6: 13-23,
1985.
5) 甲畑俊郎,劉 樹林,井戸好美,藪内英子:グラム陽性および陰性細菌 28 菌種と酵母 1
菌種に対するポビドンヨードの殺菌効果.化学療法の領域 3: 133-139. 1987.
6) 長野和代,小林寅吉吉:各種細菌および酵母様真菌に対するポビドンヨード(ネオヨジ
ン液)の殺菌効果.医薬ジャーナル 24: 325-328, 1988.
7) 川名林治,北村 敬,千葉峻三,中込 治他:ポビドンヨード(PVP-I)によるウイルス
の不活化に関する研究-市販の消毒剤との比較.臨床とウイルス 26: 371-386, 1988.
8) 中谷 一:PVP-Iodine(Isodine)による眼科手術領域の消毒.眼紀 32: 1638-1644, 1981.
9) 日下俊次,寺田勝彦,中田 裕,今居寅男他:ポビドンヨード点眼による結膜嚢消毒効
果について.眼科手術 5: 163-166, 1992.
10) 戸塚伸吉,泉 幸子,阿久津美由紀,藤沢邦見他:術前無菌法としてのポビドンヨード
による結膜嚢洗浄の意義.あたらしい眼科 14: 113-115, 1997.
11) International Organization for Standardization: Manuscript for ISO/FDIS 14729, ophthalmic
optics - Contact lens care products - Microbiological requirements and test methods for products
and regimens for hygienic management of contact lens, 2000.
12) Efron N: Microbial infiltrative keratitis. Contact Lens Complications, 1st Ed, 116-125, Optician,
Woburn, MA, 1999.
13) Sharma S, Gopalakrishnan S, Aasuri MK, Garg P et al: Trends in contact lens-associated
microbial keratitis in Southern India. Ophthalmology 110: 138 -143, 2003.
14) Rosenthal RA, Sutton SV & Schlech BA:Review of standard for evaluating the effectiveness of
contact lens disinfectants. PDA J Pharm Sci Technol 56: 37- 50, 2002.
15) Li SL, Ladage PM, Yamamoto T, Petroll WM et al:Effects of contact lens care solutions on
surface exfoliation and bacterial binding to corneal epithelial cells. Eye Contact Lens 29: 27-30,
2003.
16) Rosenthal RA, McDonald MM, Schlitzer RL, Abshire R et al: Loss of bactericidal activity from
contact lens storage solutions. CLAO J 23: 57- 62, 1997.
17) Gatti S, Cevini C, Bruno A, Penso G et al: In vitro effectiveness of povidone-iodine on
Acanthamoeba isolates from human cornea. Antimicrob Agents Chemother 42: 2232 - 2234,
1998.
(2004 年 6月 7日受付)
Comparison of the Antiviral and Anti-Acanthamoeba Effects of a
Disinfectant Solution Containing Povidone-Iodine and Three
Other Solutions
Ryoji Yanai
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Department of Ophthalmology, Toyota Chuo Hospital
Kiichi Ueda
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Shimonoseki City (Ueda Eye Clinic)
Motoharu Tajiri, Toru Matsumoto, Shigeru Nakamura and Fumio Saito
Ophtecs Corporation Research Center
Teruo Nishida
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine
Comparison of the Antiviral and Anti-Acanthamoeba Effects of a
Disinfectant Solution Containing Povidone-Iodine and Three Other
Solutions Ryoji Yanai
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Department of Ophthalmology, Toyota Chuo Hospital
Kiichi Ueda
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine and Shimonoseki City (Ueda Eye Clinic)
Motoharu Tajiri, Toru Matsumoto, Shigeru Nakamura and Fumio Saito
Ophtecs Corporation Research Center
Teruo Nishida
Department of Biomolecular Recognition and Ophthalmology, Yamaguchi University School of
Medicine
We compared the disinfectant effects of a solution for contact lens care that contained povidone-iodine
(PVP-I) with the effects of 3 other solutions for contact lens care, specifically those containing
hydrogen peroxide, polydronium, or polyhexanide, for their effects against 2 species of
Acanthamoeba and 2 viruses. The solution containing PVP-Ⅰ demonstrated disinfectant effects
equivalent to heat disinfection against Acanthamoeba polyphaga, Acanthamoeba castellanii,
adenovirus type 8, and herpes simplex virus type 1. However, the solutions containing polydronium
or polyhexamide had no effects against these organisms. The solution containing hydroxy peroxide
showed antiviral effects against herpes simplex virus type 1. These results suggest that contact lens
solutions that include PVP-I are optimal for disinfection of soft contact lenses because of their
antimicrobial activity against Acanthamoeba and viruses.
(J Jpn CL Soc 47:37-41,2005) Key Words : Povidone-Iodine(PVP-I), Chemical Disinfection, Lens Care, Acanthamoeba, Virus
Introduction
Acanthamoeba are free-living protozoa that are widely distributed in nature, including freshwater and
soil environments. Keratitis caused by Acanthamoeba is an intractable corneal infection, and its
incidence has been increasing since the first reported case in the UK in 1974. Acanthamoeba keratitis is
frequently observed in individuals who wear contact lenses, and has been primarily attributed to the use
of contact lens storage solution prepared using tap water and well water. In recent years, the use of
multipurpose solutions is increasing and accordingly, disinfectant solutions for soft contact lenses with
a reduced disinfecting capacity seem to increase the risk of Acanthamoeba infection. When a person
develops Acanthamoeba keratitis, early diagnosis and treatment are important, requiring differential
diagnosis of Acanthamoeba keratitis from herpes keratitis at the early stage. Initial infection by herpes
simplex virus occurs in childhood primarily in the lips, oral cavity, eyelids, and conjunctiva. Most adult
individuals have latent infections, which are generally asymptomatic. Recurrent herpes keratitis occurs
by reactivation of herpes virus under immunocompromised conditions, such as common colds, fever,
and stress. This type of disease can be further classified into epithelial, parenchymal, and nutritional
forms. One epithelial disease is dendritic keratitis, which requires careful diagnosis because it may be
mistaken for pseudodendritic keratitis due to Acanthamoeba infection. Adenovirus is the most common
cause of viral keratoconjunctival diseases encountered in routine practice, and is an important causative
organism for epidemic ophthalmological infections. In the prevention of viral keratoconjunctival
diseases, it is important to wash hands and disinfect tools, as in the prevention of other infections, and
to take precautions against viral infection via contact lenses when appropriate.
Povidone-iodine (PVP-I) is an iodine antiseptic with a broad spectrum of antimicrobial action against
proliferating bacteria, spores, tubercle bacilli, viruses, and fungi,1-6) and is commonly used to disinfect
fingers and surgical field skin areas.7-9) Chemical disinfectant products containing PVP-I as the antiseptic
component have recently become available for practical use in Japan. These products show superior
disinfecting effects against bacteria and fungi, and also act quickly.
In the present study, we evaluated the efficacy of a chemical disinfectant product containing PVP-I
against Acanthamoeba and viruses by comparing its disinfectant effect with the effects of a conventional
hydrogen peroxide-based product and multipurpose disinfectant products containing polidronium
chloride or polyhexanide chloride, as well as boiling disinfection by heating.
Methods
1. Test solutions
A PVP-I-based disinfectant product (Ophtecs Corp., Kobe, Japan), a hydrogen peroxide-based
disinfectant product (AMO Japan Ltd., Tokyo, Japan), a polidronium chloride-based disinfectant
product (Alcon Japan Ltd., Tokyo, Japan), and a polyhexanide chloride-based disinfectant product
(AMO Japan Ltd.) were used as the test solutions.
Solutions of 0.003% sodium sulfite and 0.01% catalase were used to neutralize PVP-I and hydrogen
peroxide, respectively, to stop the disinfecting reaction. While neutralization is not required for
disinfectant products containing polidronium chloride or polyhexanide chloride in routine lens care,
neutralization by LP solution [0.7% lecithin and 0.5% polysorbate 80 added to a 100-fold dilution of a
saline solution for amoeba (12.0 g of NaCl, 0.35 g of KCl, 0.30 g of CaCl2, 0.40 g of MgSO4•7H2O
dissolved in 1 L of 50 mM Tris-HCl buffer solution, pH 6.8)] was used in the test against amoebae or
an Eagle's Minimal Essential Medium containing 10% fetal bovine serum in the test against viruses to
stop the disinfecting reaction.11)
2. Testing the disinfectant effect against amoebae
1) Test amoeba strains
The representative strains causing Acanthamoeba keratitis, Acanthamoeba polyphaga (ATCC 30461)
and A. castellanii (ATCC 30868), which have been reported as corneal isolates, were selected.
Escherichia coli (IFO 3972) was used as a feed in the culture of Acanthamoeba strains, and the test
results were analyzed as follows by reference to the stand-alone test described in ISO 1472911).
2) Seed stock preparation
Acanthamoeba cells were cultured by feeding with E. coli on agar plate medium containing 0.01%
malt extract and 0.01% yeast extract (MY medium) for at least 4 weeks. After confirming cyst formation,
amoeba cysts were collected using the saline solution for amoebae, washed by centrifugation, and
resuspended to a concentration of 105 to 106 cysts/mL.
3) Amoeba cell counting
A 10-fold dilution series was prepared from the test amoeba solution using the saline solution for
amoebae. To each well of a multi-well plate, an appropriate amount of E. coli-containing-MY medium
and 100 μL of an amoeba dilution was added (4 wells per dilution). After incubation of the plate at 25°C
for 14 days, amoeba growth in each well was checked under a microscope, and the number of viable
cysts was calculated following the method of Reed & Muench.12)
4) Assay of disinfectant effect
To each test disinfectant solution, seed stock was added to an amount equivalent to 1% of the test
disinfectant solution to initiate disinfection. After the minimum disinfection time specified for each
disinfectant elapsed (Table 1), the test disinfectant solution was collected and added to the neutralizing
solution, and the number of viable amoeba cysts was determined in the neutralized solution. For boiling
disinfection, an appropriate amount of the saline solution for amoeba-containing seed stock was added
to a boiling case, which was sterilized in a boiler, and the number of viable amoeba cysts was determined.
As a control, the number of viable amoeba cysts was determined in the saline solution for amoeba-
containing seed stock as the loaded cyst number.
Table 1 Recommended disinfection time for chemical disinfectants
Test disinfectant solution Disinfection time
Povidone-iodine-based disinfectant product ≥5 minutes
Hydrogen peroxide-based disinfectant product ≥10 minutes
Polidronium chloride-based disinfectant product ≥4 hours
Polyhexanide chloride-based disinfectant product ≥4 hours
3. The disinfectant effect against viruses
1) Test virus strains
Adenovirus type 8 (ATCC VR-1368) and herpes simplex virus type 1 (HSV-1; ATCC VR-260) were
selected as test virus strains and HeLa cells (RCB 0007) and Vero cells (RCB 0001) were used as host
cells, respectively.
2) Seed stock preparation
For adenovirus type 8, monolayer HeLa cell cultures were infected with the virus and incubated in a
CO2 incubator until a cytopathic effect (hereinafter "CPE") was microscopically observed throughout
the monolayer. The infected cells were collected as a suspension, which was centrifuged at
approximately 2,000 × g for 10 minutes at 4°C. The pellet was resuspended in phosphate buffer,
sonicated, and used as the adenovirus type 8 seed stock to test the disinfectant effect.
For HSV-1, monolayer Vero cell cultures on the bottom of cell culture flasks were infected with HSV-
1 and incubated in a CO2 incubator until CPE was microscopically observed throughout the monolayer.
The infected cells were collected as a suspension, which was centrifuged at approximately 2,000 × g for
10 minutes at 4°C. The supernatant was diluted 10-fold in phosphate buffer, and used as the HSV-1 seed
stock to test the disinfectant effect.
4. Assay of disinfectant effects
Each test disinfectant solution was mixed with the viral seed stock, allowed to react at 25°C for the
recommended disinfection time (Table 1), and added to neutralizing solution to stop the disinfecting
reaction. Subsequently, the 50% tissue culture infectious dose (TCID50) of the residual viral titer was
determined using the calculation method of Reed & Muench12) based on the viral titer remaining in the
test sample. For boiling disinfection, an appropriate amount of phosphate buffer and the seed stock was
added to a boiling case, which was sterilized in a boiler, and the viral titer was determined.
Results
1. Disinfectant effect against amoebae
The log reduction data for A. polyphaga treated with various chemical disinfectants are presented in
Figure 1. The PVP-I-based disinfectant product resulted in an approximately 2-log reduction in cell
count, which was equivalent to the effect of boiling disinfection (2.06-log reduction). Hydrogen
peroxide-, polidronium chloride-, and polyhexanide chloride-based disinfectant products resulted in
slight reductions in cyst counts (0.61-, 0.72-, and 0.72-log reductions, respectively), demonstrating an
insufficient disinfectant effect.
Figure 1 Disinfectant effect against Acanthamoeba polyphaga
The PVP-I-based disinfectant solution also exhibited a disinfectant effect against A. castellanii,
resulting in a 2.28-log reduction in cell counts, which was similar to the effect of boiling disinfection
(i.e., a 2.28-log reduction). Other disinfectant solutions showed little or no disinfectant effects with a
log reduction of 0 to 0.5 (Figure 2).
Figure 2 Disinfectant effect against Acanthamoeba castellanii
2. Disinfectant effect against viruses
The PVP-I-based disinfectant solution showed a disinfectant effect against adenovirus type 8,
resulting in a 1.94-log reduction in viral titers, which was equivalent to the level of viral inactivation
observed for boiling disinfection (2.0-log reduction). However, hydrogen peroxide-, polidronium
chloride-, and polyhexanide chloride-based disinfectant solutions demonstrated little or no viral
inactivation in the minimum disinfection time, resulting in log reductions of 0.44, 0.0, and 0.0,
respectively (Figure 3).
(log cysts/mL)
Povidone-iodine
disinfectant
product
Log
red
uct
ion
of
mic
robia
l
cou
nt
Hydrogen
peroxide
disinfectant
product
Polidronium
chloride
disinfectant
product
Polyhexanide
chloride
disinfectant
product
Control Boiling
disinfection
(log cysts/mL)
Povidone-iodine
disinfectant
product
Log
red
uct
ion
of
mic
robia
l
cou
nt
Hydrogen
peroxide
disinfectant
product
Polidronium
chloride
disinfectant
product
Polyhexanide
chloride
disinfectant
product
Control Boiling
disinfection
Figure 3 Disinfectant effect against adenovirus type 8
PVP-I- and hydrogen peroxide-based disinfectant solutions exhibited disinfectant effects against
HSV-1 in the minimum disinfection time, resulting in log reductions of 2.22 and 2.67 for viral titers,
respectively, similar to the effect of boiling disinfection (3.22-log reduction). However, polidronium
chloride- and polyhexanide chloride-based disinfectant solutions did not show viral inactivation,
resulting in 0.04 and 0.54 log-reductions, respectively (Figure 4).
Figure 4 Disinfectant effect against herpes simplex virus type 1
Discussion
In the present study, we compared disinfectant effects of a PVP-I-based chemical disinfectant solution
against Acanthamoeba and viruses with those of conventional chemical disinfection methods. The PVP-
I-based disinfectant solution demonstrated sufficiently high disinfectant effects against all tested
microbial strains, i.e., A. polyphaga, A. castellanii, adenovirus type 8, and HSV-1, and the effect was
equivalent to that of boiling disinfection, which uses heat to kill microbes (Table 2). In contrast, the
hydrogen peroxide-based disinfectant solution and multipurpose solutions showed insufficient
disinfectant effects against Acanthamoeba and viruses within the recommended disinfection time,
(log cysts/mL)
Povidone-iodine
disinfectant
product
Log
red
uct
ion
of
mic
robia
l
cou
nt
Hydrogen
peroxide
disinfectant
product
Polidronium
chloride
disinfectant
product
Polyhexanide
chloride
disinfectant
product
Control Boiling
disinfection
(log cysts/mL)
Povidone-iodine
disinfectant
product
Log
red
uct
ion
of
mic
robia
l
cou
nt
Hydrogen
peroxide
disinfectant
product
Polidronium
chloride
disinfectant
product
Polyhexanide
chloride
disinfectant
product
Control Boiling
disinfection
indicating that these solutions were inappropriate for the prevention of infection by these
microorganisms (Table 2).
Table 2 Disinfectant effect of chemical disinfectant solutions
Amoeba Virus
AP AC ADV8 HSV-1
Povidone-iodine-based disinfectant product + + + +
Hydrogen peroxide-based disinfectant product - - - +
Polidronium chloride-based disinfectant product - - - -
Polyhexanide chloride-based disinfectant product - - - -
AP = Acanthamoeba polyphaga, AC = Acanthamoeba castellanii, ADV8 = adenovirus type 8, HSV-1 = herpes simplex virus
type1
Acanthamoeba keratitis is attributed to the use of contact lenses in more than 80% of cases reported
in Japan, and the number of patients is increasing as the number of contact lens wearers is increasing.
For this disease, there is no established treatment at present and the prevention of infection is very
important. Individuals wearing soft contact lenses should kill Acanthamoeba to a level that does not
cause infection in the daily disinfection of their contact lenses. However, chemical disinfectant products
that are widely used are not necessarily tested against Acanthamoeba, and boiling disinfection is the
most secure method for lens disinfection. PVP-I is an antiseptic reported to be useful for killing amoebae
and inactivating viruses.13,14) In the present study, we also observed a high disinfectant effect of the PVP-
I-based product, supporting its clinical effectiveness.
PVP-I is also recommended as an antiseptic for disinfecting fingers and tools in the prevention of
adenoviral conjunctivitis,15) and its effectiveness has been clinically well established. Our study provides
evidence for its effectiveness in soft contact lens disinfection against not only adenovirus but also herpes
virus. We have previously reported the effectiveness of PVP-I disinfectant products in lens disinfection
against bacteria and fungi. Combined with the results of the present study, PVP-I disinfectant products
are highly effective in soft contact lens disinfection with a broad spectrum of antimicrobial action against
bacteria, fungi, Acanthamoeba, and viruses.
In summary, the PVP-I-based chemical disinfectant product had a higher disinfectant effect against
Acanthamoeba and viruses than conventional chemical disinfection methods. Combined with the results
of our previous report, the PVP-I-based product is useful for disinfecting soft contact lenses
contaminated with a wide range of microorganisms, including bacteria, fungi, Acanthamoeba, and
viruses.
文献
1) 安生紗枝子,加賀美操,佐藤たか子,大倉真知子他:病院で常用されている消毒薬のグ
ラム陰性桿菌感染症および opportunistic infectionの原因菌となる菌種に対する殺菌作用.
防菌防微 5: 204-208, 1977.
2) 加賀谷けい子,谷口啓子,深沢義村,西川武二:ポビドンヨードの病原性酵母に対する
殺菌効果.真菌誌 21: 286-292, 1980.
3) Rackur H:New aspects of mechanism of action of povidone-iodine. J Hospital Infect 6:13 - 23,
1985.
4) 甲畑俊郎,劉 樹林,井戸好美,藪内英子:グラム陽性および陰性細菌 28 菌種と酵母 1
菌種に対するポビドンヨードの殺菌効果.化学療法の領域 3: 133-139. 1987.
5) 長野和代,小林寅吉吉:各種細菌および酵母様真菌に対するポビドンヨード(ネオヨジ
ン®液)の殺菌効果.医薬ジャーナル 24: 325 - 328, 1988.
6) 川名林治,北村 敬,千葉峻三,中込 治他:ポビドンヨード(PVP-I)によるウイルス
の不活化に関する研究-市販の消毒剤との比較.臨床とウイルス 26: 371-386, 1988.
7) 中谷 一:PVP-Iodine(Isodine)による眼科手術領域の消毒.眼紀 32: 1638-1644, 1981.
8) 日下俊次,寺田勝彦,中田 裕,今居寅男他:ポビドンヨード点眼による結膜嚢消毒効
果について.眼科手術 5: 163-166, 1992.
9) 戸塚伸吉,泉 幸子,阿久津美由紀,藤沢邦見他:術前無菌法としてのポビドンヨード
による結膜嚢洗浄の意義.あたらしい眼科 14: 113-115, 1997.
10) 柳井亮二,植田喜一,田尻大治,松本 融他:細菌・真菌に対するポビドンヨード製剤
の有効性.日コレ誌 47: 32-36, 2005.
11) International Organization for Standardization:Manuscript for ISO/FDIS 14729, ophthalmic
optics - Contact lens care products - Microbiological requirements and test methods for products
and regimens for hygienic management of contact lens, 2000.
12) Reed LJ & Muench H:A simple method of estimating fifty percent endpoints. Am J Hyg 27: 493-
497, 1938.
13) 田原和子,浅利誠志,下村嘉一,遠藤卓郎他:Acanthamoeba cystに有効な治療薬剤の検
討.感染症学雑誌 71: 1025-1030, 1997.
14) Gatti S, Cevini C, Bruno A, Penso G et al: In vitro effectiveness of povidone-iodine on
Acanthamoeba isolates from human cornea. Antimicrob Agents Chemother 42:2232-2234, 1998.
15) 薄井紀夫:ウイルス性結膜炎のガイドライン第 6章 院内感染対策.日眼会誌 107: 27-
32, 2003.
(2004 年 6月 7日受付)
Evaluation of povidone-iodine as a disinfectant solution for
contact lenses: Antimicrobial activity and cytotoxicity for
corneal epithelial cells
Ryoji Yanai a,*, Naoyuki Yamada a, Kiichi Ueda a, Motoharu Tajiri b,Toru Matsumoto b, Keiji Kido b, Shigeru Nakamura b,
Fumio Saito b, Teruo Nishida a
a Department of Biomolecular Recognition and Ophthalmology,
Yamaguchi University School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi 755-8505, Japanb Ophtecs Corporation Research Center, Toyooka, Hyogo, Japan
Abstract
Povidone-iodine (PVP-I) possesses broad-spectrum antimicrobial activity and is used clinically as a disinfectant. We evaluated the
disinfectant properties and safety of PVP-I for use as a contact lens solution. The concentrations of PVP-I required to reduce the number of
Staphylococcus aureus or Candida albicans by 3 log units were lower than were those of hydrogen peroxide, polyhexamethylene biguanide
(PHMB), and benzalkonium chloride (BAK). The cytotoxicity of PVP-I for cultured human corneal epithelial (HCE) cells was less than that
of the other three agents. The safety margin for PVP-I was thus greatest among the tested compounds. PVP-I appears suited for use as a contact
lens disinfectant.
# 2006 British Contact Lens Association. Published by Elsevier Ltd. All rights reserved.
Keywords: Soft contact lens; Disinfection; Povidone-iodine; Hydrogen peroxide; Multipurpose solution; Safety margin
www.elsevier.com/locate/clae
Contact Lens & Anterior Eye 29 (2006) 85–91
1. Introduction
Cleaning and disinfection of contact lenses are essential
for their safe wearing [1]. Disinfection is especially
important for soft contact lenses in order to avoid lens-
related infection of the cornea [2–5]. The incidence of
microbial keratitis induced by wearing of contact lenses is
3.5–14.0 cases per 10,000 individuals for daily-wear
hydrogel lenses and 20.0–144.6 cases per 10,000 indivi-
duals for extended-wear hydrogel lenses [6–8]. Although
the frequency of this condition is relatively low, it is sight
threatening and can be avoided by proper lens handling and
management [9]. The heat-based system was the first
method approved for disinfection of soft contact lenses and
has remained the most efficient [10,11]. This system has
disadvantages, however, including its induction both of lens
* Corresponding author. Tel.: +81 836 22 2277; fax: +81 836 29 2228.
E-mail address: [email protected] (R. Yanai).
1367-0484/$ – see front matter # 2006 British Contact Lens Association. Publi
doi:10.1016/j.clae.2006.02.006
deformation and of deposition of denatured proteins [12].
To avoid such problems associated with heat, a chemical
disinfection system based on hydrogen peroxide was
introduced [13]. Although hydrogen peroxide is effective
against a broad range of microbes, neutralization is required
to avoid serious insults to the ocular surface. This
neutralization step is a disadvantage in terms of compliance
[14,15]. Multipurpose disinfectant solutions, which contain
cleaning, rinsing, and disinfectant agents in a single
solution, were developed to resolve such problems.
Currently, multipurpose disinfectant solutions are used
widely, but the antimicrobial activity of these solutions is
not as great as that of heat- or hydrogen peroxide-based
disinfection systems [16–18]. The development of a new
disinfection system with an increased and broader spectrum
antimicrobial activity, with a reduced impact on contact lens
materials, and with a low cytotoxicity at the ocular surface is
thus desirable to ensure the comfort and safety of soft
contact lenses.
shed by Elsevier Ltd. All rights reserved.
R. Yanai et al. / Contact Lens & Anterior Eye 29 (2006) 85–9186
Povidone-iodine (PVP-I) is an iodinated polyvinyl
polymer that has been used as a topical antiseptic to
prevent infections of the skin or mucous membranes
during surgery [19,20]. PVP-I possesses broad-spectrum
antimicrobial activity against bacteria, yeasts, molds, other
fungi, Acanthamoeba, and certain viruses [21–24], but it
has a low toxicity to human cells and tissues [25]. On the
basis of its low toxicity at the ocular surface, a 5% solution
of PVP-I has been applied as an antiseptic before
intraocular surgery and has been shown to markedly
reduce the abundance of the conjunctival bacterial flora
[26–29]. No toxic effects of such irrigation on the ocular
surface were observed.
To evaluate the efficacy of PVP-I as a contact lens
disinfectant, we have now examined both its antimicrobial
activity against the bacterium Staphylococcus aureus and
the fungus Candida albicans as well as its cytotoxicity
toward cultured human corneal epithelial (HCE) cells. PVP-
I was compared in these tests with hydrogen peroxide and
the major chemical components of multipurpose solutions,
polyhexamethylene biguanide (PHMB) and benzalkonium
chloride (BAK).
2. Methods
2.1. Growth of microorganisms
S. aureus (Institute for Fermentation at Osaka (IFO)
13276) was grown on soybean-casein digest agar (Nihon
Pharmaceutical, Kanagawa, Japan) at 35 8C for 18–24 h,
and C. albicans (IFO1594) was cultured on Sabouraud
dextrose agar (Becton Dickinson, Franklin Lakes, NJ) at
25 8C for 42–48 h. The microbial cells were harvested with
Dulbecco’s phosphate-buffered saline (PBS), and the cell
suspension was transferred to a sterile syringe attached to a
sterile absorbent cotton pad and was centrifuged at 2000 rpm
for 10 min at 25 8C. The pellet was resuspended in PBS, and
the optical density at 660 nm of the resulting suspension was
measured with a single-beam spectrophotometer (U-2000A;
Hitachi, Tokyo, Japan). The final inoculum was adjusted to a
density of 1 � 107 to 1 � 108 colony-forming units (CFU)
per milliliter.
2.2. Culture of a human corneal epithelial cell line
An HCE cell line that had been transformed with a simian
virus 40-adenovirus recombinant vector was kindly pro-
vided by Araki-Sasaki et al. [30]. The cells were cultured in
supplemented hormone epithelial medium (SHEM), con-
sisting of Dulbecco’s modified Eagle’s medium–Ham’s F12
(50:50, v/v) (Invitrogen, Carlsbad, CA) supplemented with
15% heat-inactivated fetal bovine serum (Invitrogen),
human recombinant insulin (5 mg/ml) (Nacalai Tesque,
Kyoto, Japan), cholera toxin (0.1 mg/ml) (Sigma–Aldrich,
St. Louis, MO), human recombinant epidermal growth
factor (10 ng/ml) (Sigma–Aldrich), 0.5% dimethyl sulfoxide
(Katayama Chemical Industries, Tokyo, Japan), and
gentamicin (40 mg/ml).
2.3. Measurement of antimicrobial activity
PVP-I (BASF Japan, Tokyo, Japan), hydrogen peroxide
(Nipponperoxide, Kanagawa, Japan), PHMB (Sanyo Che-
mical Industries, Kyoto, Japan), and BAK (Tokyo Kasei
Kogyo, Tokyo, Japan) were tested for antimicrobial activity
against challenge organisms based on the current ISO
guidelines [31,32]. PVP-I (0.05–50,000 ppm), hydrogen
peroxide (3–300,000 ppm), PHMB (0.1–1000 ppm), and
BAK (0.2–2000 ppm) at various concentrations in PBS
(16 ml) were placed individually in test tubes, and 0.16 ml of
a suspension of S. aureus (log[mean number of orga-
nisms � S.D.]: 5.23 � 0.058 for PVP-I, 5.47 � 0.416 for
hydrogen peroxide, 5.40 � 0.300 for PHMB, 5.17 � 0.321
for BAK) or C. albicans (log[mean number of orga-
nisms � S.D.]: 5.83 � 0.058 for PVP-I, 5.80 � 0 for
hydrogen peroxide, 5.97 � 0.058 for PHMB,
5.87 � 0.231 for BAK) was inoculated into the tubes at
time zero. The tubes were incubated at 25 8C for 30 s–24 h;
at various times, 1 ml of each solution was removed and
added to 9 ml of neutralizing solution (sodium sulfite
[Kishida Chemical, Osaka, Japan] for PVP-I; catalase
[Nagase ChemteX, Osaka, Japan] for hydrogen peroxide; D/
E Neutralizing Broth [Becton Dickinson] for PHMB and
BAK) and incubated for 10 min at room temperature.
Portions (1 ml) of the mixtures were removed and serially
diluted with PBS, and 1 ml of each dilution was then plated
on culture agar (soybean-casein digest agar for S. aureus;
glucose-peptone digest agar for C. albicans) in triplicate.
The cultures were incubated for 5 days at 35 8C for S. aureus
and at 25 8C for C. albicans, after which the numbers of
colonies were counted and used to determine the log
reduction in CFU per milliliter. According to the ISO 14729
guidelines [13], a reduction in live S. aureus of �99.9% (3
log units) and a reduction in live C. albicans of�90% (1 log
unit) represent significant disinfectant activity. However, we
determined the concentrations of each agent required to
reduce the number of live S. aureus and C. albicans by 3 log
units.
2.4. Evaluation of cytotoxicity
Cytotoxicity of each disinfectant was examined by
staining with neutral red, which is incorporated into the
lysosomes of viable cells [33]. HCE cells were cultured
under 5% CO2 for 3 days at 37 8C in 48-well culture plates
(Coster, Corning, NY) at a density of 2 � 104 cells per well
in SHEM. The medium was then removed, and the
subconfluent cells were washed twice with SHEM before
incubation for 5 s–30 min at 37 8C in the CO2 incubator with
various concentrations of PVP-I (10–50,000 ppm), hydro-
gen peroxide (30–30,000 ppm), PHMB (1–10,000 ppm), or
R. Yanai et al. / Contact Lens & Anterior Eye 29 (2006) 85–91 87
BAK (10–1,000 ppm) in 0.2 ml of PBS in triplicate. The
cells were then washed twice with PBS and incubated for 3 h
at 37 8C with 0.005% neutral red in SHEM (0.2 ml). After
washing the cells twice with PBS, the dye was extracted for
15 min with 0.2 ml of a solution containing 1% acetic acid
and 50% ethanol. The extract was mixed thoroughly to
dissolve the neutral red crystals and its fluorescence
intensity was rapidly measured at excitation and emission
wavelengths of 530 and 580 nm. The concentration of
disinfectant required to reduce the intensity of neutral red
staining by 50% (NR50) relative to the level of staining
observed with cells treated only with PBS was calculated
[34].
2.5. Calculation of safety margin
To estimate the clinical efficacy of each chemical, we
calculated the ratio of the NR50 to the concentration required
to reduce the number of microorganisms by 3 log units for
both S. aureus and C. albicans for incubations of 30 min.
3. Results
We first examined the disinfectant activities of PVP-I,
hydrogen peroxide, PHMB, and BAK against S. aureus
(Fig. 1) and C. albicans (Fig. 2). All four chemicals
manifested antimicrobial activity in a concentration- and
time-dependent manner. PVP-I achieved a complete kill
(reduction in the number of viable microorganisms of 5–6
log units) within 30 s at 50 ppm for S. aureus (Fig. 1A) and
at 500 ppm for C. albicans (Fig. 2A), but it did not show a
disinfectant effect at 0.5 ppm for S. aureus or at 5 ppm for C.
albicans during incubation for 24 h. Hydrogen peroxide
Fig. 1. Antimicrobial activity of PVP-I (A), hydrogen peroxide (B), PHMB (C),
representative experiment.
achieved a complete kill within 30 s at 300,000 ppm for both
microorganisms (Figs. 1B and 2B). PHMB at 1,000 ppm
required 30 min for S. aureus and 1 h for C. albicans to
achieve a complete kill (Figs. 1C and 2C). BAK achieved a
complete kill within 30 s for S. aureus and within 5 min for
C. albicans at 2,000 ppm, but it did not show a marked
disinfectant effect at 2 ppm with either microorganism
during incubation for 24 h (Figs. 1D and 2D).
All four chemical agents manifested cytotoxity for HCE
cells in a concentration- and time-dependent manner
(Fig. 3). Whereas PVP-I exhibited antimicrobial activity
against S. aureus and C. albicans at concentrations of �5
and �50 ppm, respectively, it did not affect the viability of
HCE cells at concentrations up to 2,000 ppm; it was
cytotoxic at concentrations of �4,000 ppm (Fig. 4). These
results demonstrated that PVP-I is effective for disinfection
of S. aureus and C. albicans at concentrations at which it is
not cytotoxic for HCE cells.
Hydrogen peroxide showed antimicrobial activity for S.
aureus and C. albicans at concentrations of �3,000 and
�30,000 ppm, respectively, whereas it manifested cytotoxi-
city toward HCE cells at concentrations of �1,200 ppm
(Fig. 5). Hydrogen peroxide was thus effective for
disinfection of S. aureus and C. albicans, but, at the
concentrations required for antimicrobial activity, it was also
cytotoxic for HCE cells.
PHMB exhibited antimicrobial activity for S. aureus and
C. albicans at concentrations of �10 and �100 ppm,
respectively, whereas it was cytotoxic for HCE cells at
concentrations of �100 ppm (Fig. 6). Thus, like hydrogen
peroxide, PHMB was cytotoxic for HCE cells at concentra-
tions required for disinfection of S. aureus or C. albicans.
BAK showed antimicrobial activity for S. aureus and C.
albicans at concentrations of �20 and �200 ppm, respec-
or BAK (D) against S. aureus. Data are means � S.D. of triplicates from a
R. Yanai et al. / Contact Lens & Anterior Eye 29 (2006) 85–9188
Fig. 2. Antimicrobial activity of PVP-I (A), hydrogen peroxide (B), PHMB (C), or BAK (D) against C. albicans. Data are means � S.D. of triplicates from a
representative experiment.
tively, aswellascytotoxicity forHCEcellsatconcentrationsof
�20 ppm (Fig. 7). The concentrations of BAK necessary for
antimicrobial activity were thus also cytotoxic for HCE cells.
PVP-I was the most potent of the tested compounds with
regard to antimicrobial activity for both S. aureus and C.
albicans, whereas hydrogen peroxide was the least potent
(Table 1). The NR50 of PVP-I for HCE cells was also the
highest among the tested agents, whereas that of BAK was
the lowest. PVP-I thus showed the highest safety margin by
Fig. 3. Cytotoxicity of PVP-I (A), hydrogen peroxide (B), PHMB (C), or BAK (D)
experiment.
far with regard to disinfection of both microorganisms and
cytotoxicity toward HCE cells.
4. Discussion
The wearing of soft contact lenses can cause infection of
the corneal or conjunctival epithelium with pathogenic
microorganisms [35]. Efficient disinfection of the lenses is
against HCE cells. Data are means � S.D. of triplicates from a representative
R. Yanai et al. / Contact Lens & Anterior Eye 29 (2006) 85–91 89
Fig. 4. Disinfectant properties and cytotoxicity of PVP-I. Antimicrobial
activity against S. aureus (closed diamonds) or C. albicans (open diamonds)
and cytotoxicity toward HCE cells (closed triangles) were determined. Data
are means � S.D. of triplicates from a representative experiment.
Fig. 6. Disinfectant properties and cytotoxicity of PHMB. Antimicrobial
activity against S. aureus (closed diamonds) or C. albicans (open diamonds)
and cytotoxicity toward HCE cells (closed triangles) were determined. Data
are means � S.D. of triplicates from a representative experiment.
thus essential for their safe use [36,37]. However, certain
disinfectant components themselves have been found to
induce keratitis [38]. It is therefore important to strike a
balance between antimicrobial activity and biocompatibility
in disinfection of soft contact lenses. We have now evaluated
both the antimicrobial activity and cytotoxicity of PVP-I for
this purpose in comparison with three chemical components
of commercially available lens disinfectant solutions. PVP-I
was not only the most effective disinfectant against both the
tested bacterium and fungus but also the least cytotoxic,
yielding the highest safety margin by far.
PVP-I has been used for many years as a broad-spectrum
antimicrobial to disinfect medical materials and supplies as
well as the human body [39]. Its microbicidal activity is
mediated by reaction with enzymes of the respiratory chain
and with amino acids of cell membrane proteins in the
microorganisms [40]. We have now evaluated the antimicro-
bial activity of PVP-I in comparison with three chemical
components of contact lens disinfectant solutions tested at
various concentrations and times that include the concentra-
tions present in the contact lens solutions (30,000 ppm for
hydrogen peroxide; 1 ppm for PHMB) and the times
recommended for incubation of lenses with these solutions
(10 min for hydrogen peroxide; 4 h for PHMB). We
determined the concentrations of PVP-I required to reduce
the number of live microorganisms by 3 log units during
30 min to be 4.17 ppm for S. aureus and 34.46 ppm for C.
albicans, values that are similar to those (0.1–1%) determined
Fig. 5. Disinfectant properties and cytotoxicity of hydrogen peroxide.
Antimicrobial activity against S. aureus (closed diamonds) or C. albicans
(open diamonds) and cytotoxicity toward HCE cells (closed triangles) were
determined. Data are means � S.D. of triplicates from a representative
experiment.
for the same organisms in a previous study [40]. Indeed, we
have recently developed a contact lens disinfection and
cleaning system containing 0.05% PVP-I (Clencide1), and
this system has been shown to be effective against bacteria,
yeast, mold, and Acanthamoeba [41–43].
According to the ISO 14729 guidelines [31], the effects of
potential disinfectants for contact lens solutions on micro-
organisms should be investigated with a suspension test. We
selected S. aureus as a representative bacterium and C.
albicans, one of the most frequent microbial causes of
keratitis [2–6,44], as a representative fungus for suspension
tests of the antimicrobial activity of PVP-I. We have
previously examined the effects of a contact lens solution
containing PVP-I (Clencide1) on all five challenge organisms
recommended by the ISO 14729 guidelines: Pseudomonas
aeruginosa, S. aureus, Serratia marcescens, Fusarium solani,
and C. albicans. Our previous study showed that the
susceptibility of C. albicans to this solution was lower than
that of the other microorganisms [42]. In addition, both S.
aureus and C. albicans derive their importance not only from
the severity of the associated infections but also from their
ability to develop resistance to antimicrobial agents [45,46].
We examined cytotoxicity toward cultured HCE cells as an
indicator of potential injury to the corneal epithelium.
Cytotoxicity was apparent at 125 ppm for PVP-I, 30 ppm for
hydrogen peroxide, 10 ppm for PHMB, and 10 ppm for BAK
during incubation with HCE cells for 30 min. To compare the
safety margin of PVP-I with those of hydrogen peroxide,
Fig. 7. Disinfectant properties and cytotoxicity of BAK. Antimicrobial
activity against S. aureus (closed diamonds) or C. albicans (open diamonds)
and cytotoxicity toward HCE cells (closed triangles) were determined. Data
are means � S.D. of triplicates from a representative experiment.
R. Yanai et al. / Contact Lens & Anterior Eye 29 (2006) 85–9190
Table 1
Antimicrobial potencies for S. aureus and C. albicans, cytotoxicity for HCE cells, and safety margins of the test compounds
Compound Antimicrobial potencya (ppm) Cytotoxicityb (ppm) Safety marginc
S. aureus C. albicans S. aureus C. albicans
PVP-I 4.17 34.46 2909 697.60 84.42
Hydrogen peroxide 8357.18 20888.78 698 0.08 0.03
PHMB 235.98 442.87 58 0.25 0.13
BAK 15.23 120.74 16 1.05 0.13
a Values are concentrations requied to reduce the number of live cells by �99.9% for both S. aureus and C. albicans.b Values are NR50 concentrations for HCE cells.c Values represent NR50/antimicrobial potency ratios.
PHMB, and BAK in the present study, we chose an exposure
time of 30 min for both microorganisms and HCE cells on the
basis of the time course data shown in Figs. 1–3.
The disinfection criteria of the ISO 14729 guidelines
require a reduction in the number of live bacteria and fungi of
3 and 1 log units, respectively. In the present study, we instead
determined the concentrations of the test agents required to
reduce the number of both live S. aureus and C. albicans
organisms by 3 log units, given that all four chemicals
achieved a complete kill of the fungus during incubation for
30 min. PVP-I and BAK showed a greater antimicrobial
potency than did hydrogen peroxide and PHMB. Although all
four tested compounds showed a concentration-dependent
cytotoxicity toward HCE cells, the NR50 values of PVP-I and
hydrogen peroxide were much larger than were those of
PHMB and BAK. Furthermore, the safety margin of PVP-I
was much higher than those of the other three agents.
Overall, our data indicate that PVP-I, which possesses
broad-spectrum antimicrobial activity and has been safely
used for ocular disinfection, is suitable for disinfection of
soft contact lenses than are other chemicals currently used
for this purpose. However, there are multiple requirements
for the use of disinfecting agents in contact lens solutions.
Further characterization of PVP-I with regard to such issues
as formulation, stability, ongoing disinfection ability, and
compatibility with contact lenses is thus warranted.
Acknowledgments
This research was supported by grants from the Japan
Society for the Promotion of Science (JSPS) and the
Ministry of Education, Culture, Sports, Science, and
Technology of Japan (to T.N.).
References
[1] Bowden 3rd FW, Cohen EJ, Arentsen JJ, Laibson PR. Patterns of lens
care practices and lens product contamination in contact lens asso-
ciated microbial keratitis. CLAO J 1989;15:49–54.
[2] Bourcier T, Thomas F, Borderie V, Chaumeil C, Laroche L. Bacterial
keratitis: predisposing factors, clinical and microbiological review of
300 cases. Br J Ophthalmol 2003;87:834–8.
[3] Cheng KH, Leung SL, Hoekman HW, Beekhuis WH, Mulder PG,
Geerards AJ, et al. Incidence of contact-lens-associated microbial
keratitis and its related morbidity. Lancet 1999;354:181–5.
[4] Dart JK, Stapleton F, Minassian D. Contact lenses and other risk
factors in microbial keratitis. Lancet 1991;338:650–3.
[5] Mah-Sadorra JH, Yavuz SG, Najjar DM, Laibson PR, Rapuano CJ,
Cohen EJ. Trends in contact lens-related corneal ulcers. Cornea
2005;24:51–8.
[6] Poggio EC, Glynn RJ, Schein OD, Seddon JM, Shannon MJ, Scardino
VA, et al. The incidence of ulcerative keratitis among users of daily-
wear and extended-wear soft contact lenses. N Engl J Med
1989;321:779–83.
[7] Efron N, Morgan PB, Hill EA, Raynor MK, Tullo AB. Incidence
and morbidity of hospital-presenting corneal infiltrative events
associated with contact lens wear. Clin Exp Optom 2005;88:
232–9.
[8] Morgan PB, Efron N, Hill EA, Raynor MK, Whiting MA, Tullo AB.
Incidence of keratitis of varying severity among contact lens wearers.
Br J Ophthalmol 2005;89:430–6.
[9] Matthews TD, Frazer DG, Minassian DC, Radford CF, Dart JK. Risks
of keratitis and patterns of use with disposable contact lenses. Arch
Ophthalmol 1992;110:1559–62.
[10] Busschaert SC, Good RC, Szabocsik J. Evaluation of thermal disin-
fection procedures for hydrophilic contact lenses. Appl Environ
Microbiol 1978;35:618–21.
[11] Pepose JS. Contact lens disinfection to prevent transmission of viral
disease. CLAO J 1988;14:165–8.
[12] Weisbarth RE, Henderson B. In: Bennet ES, Weissman BA, editors.
Clinical contact lens practice. Philadelphia: Lippincott Williams &
Wilkins; 2005. p. 381–419.
[13] Gasset AR, Ramer RM, Katzin D. Hydrogen peroxide sterilization of
hydrophilic contact lenses. Arch Ophthalmol 1975;93:412–5.
[14] Harris MG, Torres J, Tracewell L. pH and H2O2 concentration of
hydrogen peroxide disinfection systems. Am J Optom Physiol Opt
1988;65:527–35.
[15] Holden B. A report card on hydrogen peroxide for contact lens
disinfection. CLAO J 1990;16:S61–4.
[16] Lowe R, Vallas V, Brennan NA. Comparative efficacy of contact lens
disinfection solutions. CLAO J 1992;18:34–40.
[17] Sickler SG, Bao N, Littlefield SA. Comparative antimicrobial activity
of three leading soft contact lens disinfection solutions. Int Contact
Lens Clin 1992;19:19–23.
[18] Hiti K, Walochnik J, Haller-Schober EM, Faschinger C, Aspock H.
Viability of Acanthamoeba after exposure to a multipurpose disin-
fecting contact lens solution and two hydrogen peroxide systems. Br J
Ophthalmol 2002;86:144–6.
[19] Furukawa K, Ogawa R, Norose Y, Tajiri T. A new surgical handwash-
ing and hand antisepsis from scrubbing to rubbing. J Nippon Med Sch
2004;71:190–7.
[20] Messager S, Goddard PA, Dettmar PW, Maillard JY. Comparison of
two in vivo and two ex vivo tests to assess the antibacterial activity of
several antiseptics. J Hosp Infect 2004;58:115–21.
R. Yanai et al. / Contact Lens & Anterior Eye 29 (2006) 85–91 91
[21] Benevento WJ, Murray P, Reed CA, Pepose JS. The sensitivity of
Neisseria gonorrhoeae, Chlamydia trachomatis, and herpes simplex
type II to disinfection with povidone-iodine. Am J Ophthalmol
1990;109:329–33.
[22] Chaudhary U, Nagpal RC, Malik AK, Kumar A. Comparative evalua-
tion of antimicrobial activity of polyvinylpyrrolidone (PVP)-iodine
versus topical antibiotics in cataract surgery. J Indian Med Assoc
1998;96:202–4.
[23] Foster A, Klauss V. Ophthalmia neonatorum in developing countries.
N Engl J Med 1995;332:600–1.
[24] Gatti S, Cevini C, Bruno A, Penso G, Rama P, Scaglia M. In vitro
effectiveness of povidone-iodine on Acanthamoeba isolates
from human cornea. Antimicrob Agents Chemother 1998;42:
2232–4.
[25] Lachapelle JM. Allergic contact dermatitis from povidone-iodine: a
re-evaluation study. Contact Dermat 2005;52:9–10.
[26] Isenberg SJ, Apt L, Yoshimori R, Khwarg S. Chemical preparation of
the eye in ophthalmic surgery. IV. Comparison of povidone-iodine on
the conjunctiva with a prophylactic antibiotic. Arch Ophthalmol
1985;103:1340–2.
[27] Apt L, Isenberg SJ, Yoshimori R, Spierer A. Outpatient topical use of
povidone-iodine in preparing the eye for surgery. Ophthalmology
1989;96:289–92.
[28] Ciulla TA, Starr MB, Masket S. Bacterial endophthalmitis prophylaxis
for cataract surgery: an evidence-based update. Ophthalmology
2002;109:13–24.
[29] The Royal College of Ophthalmologists. Published guidelines. Catar-
act surgery Guidelines. 2004.
[30] Araki-Sasaki K, Ohashi Y, Sasabe T, Hayashi K, Watanabe H, Tano
Y, et al. An SV40-immortalized human corneal epithelial cell line
and its characterization. Invest Ophthalmol Vis Sci 1995;36:614–
21.
[31] International Organization for Standardization. ISO 14729. Ophthal-
mic optic-contact lens care products–microbiological requirements
and test methods for products and regimens for hygienic management
of contact lenses. 2001.
[32] Kramer A, Rudolph P, Werner HP. Antimicrobial efficacy of contact
lens care products and critical comment on ISO/FDIS 14729. Dev
Ophthalmol 2002;33:343–61.
[33] Borenfreund E, Puerner J. A simple quantitative procedure using
monolayer cultures for cytotoxicity assays (HTD/NR-90). Tissue Cult
Methods 1984;9:7–9.
[34] Nakamura S, Shibuya M, Saito Y, Nakashima H, Saito F, Higuchi A,
et al. Protective effect of D-beta-hydroxybutyrate on corneal epithelia
in dry eye conditions through suppression of apoptosis. Invest
Ophthalmol Vis Sci 2003;44:4682–8.
[35] Seal DV, Kirkness CM, Bennett HG, Peterson M, Keratitis Study
Group. Population-based cohort study of microbial keratitis in Scot-
land: incidence and features. Contact Lens Anter Eye 1999;22:49–57.
[36] Ky W, Scherick K, Stenson S. Clinical survey of lens care in contact
lens patients. CLAO J 1998;24:216–9.
[37] Rosenthal RA, Henry CL, Schlech BA. Contribution of regimen steps
to disinfection of hydrophilic contact lenses. Contact Lens Anter Eye
2004;27:149–56.
[38] Soni PS, Horner DG, Ross J. Ocular response to lens care systems in
adolescent soft contact lens wearers. Optom Vis Sci 1996;73:70–85.
[39] Burks RI. Povidone-iodine solution in wound treatment. Phys Ther
1998;78:212–8.
[40] Rackur H. New aspect of mechanisim of povidone-iodine. J Hosp
Infect 1985;6:13–23.
[41] Kilvington S. Antimicrobial efficacy of a povidone iodine (PI) and a
one-step hydrogen peroxide contact lens disinfection system. Contact
Lens Anter Eye 2004;27:209–12.
[42] Yanai R, Ueda K, Tajiri M, Matsumoto T, Nakamura S, Saito F, et al.
Comparison of the antibacterial and antifungal effects of a contact lens
solution containing povidone-iodide and three other solutions. J Jpn
Contact Lens Soc 2005;47:32–6.
[43] Yanai R, Ueda K, Tajiri M, Matsumoto T, Nakamura S, Saito F, et al.
Comparison of the antiviral and anti-acanthamoeba effects of a
disinfectant solution containing povidone-iodide and three other
solutions. J Jpn Contact Lens Soc 2005;47:37–41.
[44] Thomas PA. Current perspectives on ophthalmic mycoses. Clin
Microbiol Rev 2003;16:730–97.
[45] Mather R, Karenchak LM, Romanowski EG, Kowalski RP. Fourth
generation fluoroquinolones: new weapons in the arsenal of ophthal-
mic antibiotics. Am J Ophthalmol 2002;133:463–6.
[46] Prasad R, Kapoor K. Multidrug resistance in yeast Candida. Int Rev
Cytol 2005;242:215–48.
The improvement of CL discomfort by a novel
povidone-iodine based disinfection systemHaruki Nakagawa, Kazuhiro Sasanuma, Katsuhide Yamasaki, Fumio Saitoh
Ophtecs Corporation, Kobe, Japan
Purpose
Materials and Methods
OPHTECS CORPORATION
Challenge and Innovation
Protecting healthy vision for all
Introduction
It is reported that more than half of SCL wearers have some discomfort feeling
while wearing SCL(CL discomfort) 1).
The causes of CL discomfort deem to include physical stimuli by SCL such as
friction, protein deposition on SCLs, meibomian gland dysfunction and lid wiper
epitheliopathy, and each factor is related intricately.
Regarding protein deposition in these factors, the relevance between increment of
discomfort or dryness feeling while wearing and amount of specific
protein(Lipocalin-1, denatured lysozyme) in tear fluid or on the lenses have been
reported by M. Willcox et al. 2) and L. Jones et al. 3)
We focused on these proteins with a view to reduce CL discomfort by CL solution.
The purpose of this study was to evaluate the influence of protein deposits on
CL discomfort (CLD) from a perspective of lens materials and CL solutions.
Soft contact lens:Etafilcon A and Balafilcon A as an ionic lens, Senofilcon A and Comfilcon A as a
non-ionic lens
Table 1. Contact lens care systems used in this study
Solution Active Neutralizer Cleaning agent Soaking time of SCL
ingredient (Disinfection time)
MPDSPHMB
(1.1ppm)None
Poloxamine,Hydroxyalkylphosphonate
4 hours
(4 hrs)
PVP-I
system
Povidone
Iodine
(0.05%)
Ascorbic
AcidProtease
4 hours
(5 mins)
Lens care solution:Contact lens care solutions used in this study are shown in Table 1.
Povidone-iodine based disinfecting and cleaning system (PVP-I system) is
comprised of the tablet containing PVP-I in the outer layer, a neutralizer and
protease in its inner core, and a dissolving and rinsing solution.
The tablet was put into the designated lens case, poured the dissolving and rinsing
solution and then soaked the lenses. After more than 4 hours, rinsed the lenses by
the dissolving and rinsing solution before wearing.
Criteria for CLD while wearing:CLDEQ-8 questionnaire4) was applied in order to digitize the degree of discomfort
feeling.
The degree and score of each five discomfort items were defined as follows.
1. Eye discomfort (frequency, intensity) : Mild (0 – 3), Moderate (4 – 6), Severe (7 – 9)
2. Eye dryness (frequency, intensity) : Mild (0 – 3), Moderate (4 – 6), Severe (7 – 9)
3. Blurry vision (frequency, intensity) : Mild (0 – 3), Moderate (4 – 6), Severe (7 – 9)
4. Closing your eyes (frequency) : Mild (0 – 1), Moderate (2), Severe (3 – 4)
5. Removing your lenses (frequency) : Mild (1 – 2), Moderate (3 – 4), Severe (5 – 6)
The relevance between CL discomfort and proteins in tear fluid and on the
lenses:Twelve participants (5 male, 7 female, Average age: 29.4±5.8) wore ionic
Etafilcon A and Balafilcon A lenses using PHMB based solution (MPDS) for 14 days
respectively. CLDEQ-8 questionnaire was applied in the evening on the 14th day,
and their tear fluid was collected by using schirmer paper strips. Then, their lenses
were soaked in TFA solution in order to extract total protein. Lipocalin-1 and
Lysozyme in these samples were assessed by using HPLC.
The relevance between the degree of discomfort and the amount of those protein
was evaluated.
Comparison with Lipocalin-1 deposits and dryness feeling by lens materials:Nine participants (4 male, 5 female, Average age: 29.5±7.2) with moderate to
severe for dryness feeling wore ionic Etafilcon A, Balafilcon A, non-ionic
Senofilcon A and Comfilcon A lenses using the MPDS for 14 days respectively.
Dryness score (CLDEQ-8) and amount of Lipocalin-1 deposition on their lenses
were measured as described above.
Comparison with NIBUT while wearing ionic and non-ionic lenses:Five participants (2 male, 3 female, Average age: 31.0±6.4) with moderate to
severe for dryness feeling wore ionic Etafilcon A and non-ionic Senofilcon A lenses
using the MPDS for 14 days respectively.
Dryness score (CLDEQ-8) and NIBUT on the lens during wearing with DR-1 was
measured in the evening of the 1st and the 14th day. Further, amount of Lipocalin-1
deposition on their lenses was assessed as described above.
Lipocalin-1 deposits, NIBUT and dryness feeling while wearing ionic lenses
with PVP-I system:Aforementioned five participants wore ionic Etafilcon A lenses using PVP-I system
and the MPDS for 14 days respectively.
NIBUT on the lens during wearing, dryness score (CLDEQ-8) and amount of
Lipocalin-1 deposition on their lenses were assessed as described above.
Results
The relevance between CLD and proteins in tear fluid and on the lenses:
A positive correlation was observed between CLD, especially dryness feeling and amount of
Lipocalin-1 in tear fluid or on the SCLs. Meanwhile, no relevance was observed between
Lysozyme and CLD. (Pearson correlation analysis) (Table 2)
The subjects who had moderate to severe dryness feeling were significantly got increased the
amount of Lipocalin-1 in their tear fluid and the deposits on their SCLs compared to subjects
with mild. (Mann Whitney U test) (Fig.1)
Lysozyme
in tear fluid
Lipocalin-1
in tear fluid
Lipocalin-1
deposits on
Etafilcon A
Lipocalin-1
deposits on
Balafilcon A
CLDEQ-8
(Total score)
0.520
(p=0.123)
0.562
(p=0.046)
0.641
(p=0.063)
0.777
(p=0.040)
Eye
discomfort
0.329
(p=0.354)
0.580
(p=0.038)
0.627
(p=0.071)
0.411
(p=0.311)
Eye dryness0.158
(p=0.663)
0.629
(p=0.021)
0.677
(p=0.045)
0.930
(p=0.001)
Blurry vision0.265
(p=0.459)
0.302
(p=0.316)
0.315
(p=0.409)
0.849
(p=0.008)
Closing
eyes
0.565
(p=0.089)
0.251
(p=0.408)
0.558
(p=0.119)
0.527
(p=0.179)
Removing
lenses
0.437
(p=0.207)
0.179
(p=0.559)
0.365
(p=0.334)
0.350
(p=0.396)
Table 2. The relevance between CLD and proteins in tear
fluid and on the lenses
References
Conclusions
3. L. Jones et al., Optometry and Vision Science, 2006, 83, 3, 143-151
2. M.D. Willcox et al., Current Eye Research, 2002, Vol.25, No.4, 227-235
4. S.B. Hickson-Curran et al., Optometry and Vision Science, 2012, Vol. 89, No. 10, 1435-1442
1. The TFOS International Workshop on Contact Lens Discomfort: Executive Summary, IOVS, October 2013, Vol. 54, No. 11
It was suggested that concentration of Lipocalin-1 in tears of SCL wearers with dryness
feeling is high, thus Lipocalin-1 easily deposited on ionic SCLs might be a cause of dryness
feeling due to destabilization of tear film.
Choosing of non-ionic SCLs or using care solutions such as PVP-I system containing
protease for SCL wearers with dryness feeling is highly recommended.
Comparison with Lipocalin-1 deposits and dryness feeling by lens materials:
Amount of Lipocalin-1 deposited on
the nonionic lenses (Senofilcon A
and Comfilcon A) were significantly
lower than the ionic lenses
(Etafilcon A and Balafilcon A), and
also dryness feeling while wearing
the nonionic lenses was significantly
lower compared to the ionic lenses.
(Fisher’s PLSD) (Fig.2)
0
1
2
3
4
5
6
7
8
9
10
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
Am
ount
of
Lip
ocalin
-1(μ
g/μ
L)
P < 0.01 P < 0.05
Score
for
dry
ness f
eelin
g
Fig. 2. Comparison with Lipocalin-1 deposits and dryness feeling
by lens materials
Comparison with NIBUT while wearing ionic and non-ionic lenses:
Amount of Lipocalin-1 deposited on
Etafilcon A lenses significantly got
higher than that of Senofilcon A
lenses, and NIBUT on Etafilcon A
lens while wearing got a significant
decrease at the 14th day compared
to the 1st day, and there was also a
significant increase in dryness score
at the 14th day. Meanwhile, no
significant differences was observed
between the 1st and the 14th day
with Senofilcon A lenses.
(Mann Whitney U test) (Fig.3)
0.0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8P < 0.05
Am
ount
of
Lip
ocalin
-1(μ
g/μ
L)
0.0
1.0
2.0
3.0
4.0
5.0
6.0
7.0
8.0
1st
day
14th
day
etafilcon A
1st
day
14th
day
senofilcon A
NIB
UT
(sec)
P < 0.05
0
1
2
3
4
5
6
7
8
P < 0.05
Score
for
dry
ness f
eelin
g1st
day
14th
day
etafilcon A
1st
day
14th
day
senofilcon A
Fig. 3. Comparison with NIBUT while wearing ionic and
non-ionic lenses
Lipocalin-1 deposits, NIBUT and dryness feeling while wearing ionic lenseswith PVP-I system
Amount of Lipocalin-1 deposited on
Etafilcon A lenses cared with PVP-I
system was significantly lower than
that of the MPDS, and no significant
differences was observed between
the 1st and the 14th day in NIBUT
and in the dryness score.
(Mann Whitney U test) (Fig.4)
0.0
1.0
2.0
3.0
4.0
5.0
6.0
7.0
8.0
9.0
Am
ount
of
Lip
ocalin
-1(μ
g/μ
L)
P < 0.05
NIB
UT
(sec)
1st
day
14th
day
MPS
1st
day
14th
day
PVP-I system
system
P < 0.05
0
1
2
3
4
5
6
7
8P < 0.05
Score
for
dry
ness f
eelin
g
1st
day
14th
day
1st
day
14th
day
MPS PVP-I system
Fig. 4. Lipocalin-1 deposits, NIBUT and dryness feeling
while wearing ionic lenses with PVP-I system
0.0
1.0
2.0
3.0
4.0
5.0
Am
oun
t o
f L
ipo
calin
-1(μ
g/μ
L)
Mild >Moderate
n=3
n=9
P < 0.05
0.0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
Am
oun
t o
f L
ipo
calin
-1(μ
g/μ
L)
n=3
n=9
n=3
n=9
P < 0.05 P < 0.05
Tear fluidDeposits on
Etafilcon A Balafilcon A
Fig. 1. The relevance between dryness feeling and Lipocalin-1 in tear fluid and on the lenses
Contact: Haruki Nakagawa ([email protected])
ARTICLE
Clinical Outcomes and Contact Lens Case ContaminationUsing a Povidone–Iodine Disinfection System
Jacqueline Tan, Ph.D., Ananya Datta, M.Phil., Katherine Wong, B.Optom., Mark D. P. Willcox, Ph.D.,and Ajay K. Vijay, Ph.D.
Objective: To assess the incidence of adverse events during the use ofa povidone–iodine disinfecting solution (cleadew) and the microbial con-tamination in contact lens cases.Methods: A prospective, single-center, open-label, controlled studyevaluating the use of cleadew cleaning and disinfecting system in existingdaily wear soft contact lens wearers over a 3-month period was conducted.Ocular signs and symptoms during lens wear were assessed at baseline andafter 1 and 3 months of using cleadew. Contact lens cases were assessed forthe frequency of microbial contamination and the types of microbes, usingtraditional microbial culture, followed by identification of bacteria using16S rRNA sequencing.Results: Use of cleadew was well tolerated. There was reduction in cornealstaining (0.560.5 at 3 months of use) compared with the participant’shabitual multipurpose disinfecting system (1.161.0); all other clinical signswere not significantly different. There were no cases of solution-inducedcorneal staining. There was a low adverse event rate of 0.8% per 100participant-months. Contact lens case contamination was low, with 30%of cases having no culturable microbes. Comparison with previously pub-lished data showed that use of cleadew resulted in low frequencies of Gram-positive (49%) and fungal (8%) contamination and a low, but higher thansome other disinfecting solutions, level of Gram-negative bacteria.Conclusions: Cleadew cleaning and disinfecting system was associatedwith low levels of adverse events during use. Contact lens cases weresignificantly less frequently contaminated than for some other types ofdisinfecting solutions.
Key Words: Povidone–iodine—Contact lens storage case—Bacteria—Comfort—Adverse events.
(Eye & Contact Lens 2017;0: 1–7)
A lmost a decade ago, global estimates indicated that therewere more than 140 million contact lens wearers world-
wide.1 Discontinuations from contact lens wear due to discomfortand dryness remain, even with contemporary lens types,2 and thishas been identified as a factor hampering growth of the contact lensmarket.3 Nevertheless, the overall number of contact lens wearersis expected to rise, given the growth in use of contact lenses to
control myopia progression in children and the uptake of multifo-cal contact lens corrections as the population ages.4,5
Contact lenses are generally considered to be a safe form of visioncorrection. However, adverse events do occur. Acute infectious andinflammatory/infiltrative complications associated with contact lenswear have been shown to present a considerable health andeconomic burden to both affected individuals and to public healthsystems. In addition to the severe pain and potential for loss of visionwith microbial keratitis, the median treatment cost for microbialkeratitis in Australia and New Zealand has been estimated at overAU$1,200, which includes both the direct cost of health care, plusindirect costs related to time off work and costs associated withassistance from a care giver.6 Although corneal infiltrative events areless severe and typically associated with discomfort and inconve-nience caused by discontinuation of contact lens wear,7 the cost percontact lens–associated corneal infiltrative event is high, rangingfrom US$1,003 to 1,496.8 Therefore, eliminating or minimizing therisk factors for developing lens-related complications is desirable forboth affected individuals and society in general.Microbial contamination of contact lens storage cases, used
during storage of lenses when not being worn, is an importantconsideration given the potential for pathogenic microorganisms inthe lens case to colonize contact lenses and be transmitted to theeye.9 Microbial colonization of contact lenses has been implicatedin contact lens–induced corneal inflammatory events.10–12 Contactlens case contamination rates range from 18% to 85%.13 In a studyexamining the incidence of noninfectious keratitis during wear ofsilicone hydrogel contact lenses, Carnt et al.7 found that the ratewas dependent on the contact lens multipurpose disinfectingsolution combination, with the lowest levels of corneal infiltrativeevents being produced when silicone hydrogel contact lenses wereused in combination with a one-step hydrogen peroxide dis-infecting system. Analysis of the contact lens cases used during theclinical trials reported by Carnt et al.7 demonstrated that lens caseswere contaminated during use,14 and a further analysis showed thatthe rate of corneal infiltrative events was correlated to the level ofmicrobial contamination of lens cases.13
Povidone–iodine (a commonly used medical disinfectant) hasbeen available as a contact lens care solution in Japan for severalyears15,16; however, no studies have reported the incidence rates ofadverse events in contact lens wearers using povidone–iodine, noron the rate of contamination of contact lens cases with this solution.Studies have demonstrated the excellent in vitro antimicrobialactivity of 5% povidone–iodine against a number of clinical strainsof Pseudomonas aeruginosa, Escherichia coli, Staphylococcusaureus (including methicillin-resistant strains), Candida albicans,
From the School of Optometry and Vision Science, University of NewSouth Wales, Sydney, Australia.
M. D. P. Willcox is a member of the Scientific Advisory Board of OphtecsCorp.The remaining authors have no conflicts of interest to disclose.
Supported by a grant from Ophtecs Corporation, Kobe, Japan.Address correspondence to Mark D. P. Willcox, Ph.D., School of Optometry
and Vision Science, University of New South Wales, Gate 14 Barker Street,Sydney, NSW 2052, Australia; e-mail: [email protected]
Accepted February 5, 2017.
DOI: 10.1097/ICL.0000000000000385
Eye & Contact Lens � Volume 0, Number 0, Month 2017 1
Copyright � Contact Lens Association of Opthalmologists, Inc. Unauthorized reproduction of this article is prohibited.
and Acanthamoeba.17–20 Many of these studies had been conductedusing the International Organisation for Standardization protocol14729, which is a requirement for testing before sale of solutions inmany countries.18–20 Versions of a povidone–iodine cleaning anddisinfecting system have been also shown to be effective againstAcanthamoeba and Fusarium when tested in vitro.15,16,21,22
The purpose of this study was to assess the incidence of adverseevents during wear of contact lenses and use of a povidone–iodinedisinfecting solution (cleadew cleaning and disinfecting system;Ophtecs Corp, Kobe, Japan), and the rate and level of contami-nation in contact lens cases.
MATERIALS AND METHODS
Clinical TrialThis was a prospective, single-center, open-label, controlled
study evaluating the use of cleadew cleaning and disinfectingsystem in existing, frequent replacement daily wear soft contactlens wearers over a 3-month period. Details of the cleadewcleaning and disinfecting system are shown in Table 1. All proce-dures were conducted in accordance with the Declaration ofHelsinki and were approved by the University of New South WalesHuman Research Ethics Committee.Silicone hydrogel and hydrogel lens wearers were included, but
people using daily disposable or gas permeable lenses or those withself-reported iodine sensitivity were excluded. Forty participants whoprovided written informed consent were dispensed with cleadewcleaning and disinfecting solution for use with a fresh (new) pair oftheir regular soft contact lenses. Participants were instructed to weartheir contact lenses for a minimum of 4 days per week on average forthe duration of the study and to replace the lenses according to themanufacturers recommended schedule. On daily removal of the lensfrom the eye, participants were advised to place lenses directly into theappropriate case compartment and close the basket. The lens case wasto be filled to the indicated line with cleadew dissolving and rinsingsolution and a cleadew tablet added to the lens case. The lens case wasto be capped and lenses left in the case for a minimum of 4 hr (themanufacturer’s recommended minimum disinfection and cleaningtime). On removal of the contact lenses from the case, participantswere instructed to rinse their lenses with the cleadew dissolving andrinsing solution before inserting lenses into their eyes. Solutions in thelens case were to be discarded, and the lens case (lens well andbaskets) was to be thoroughly rinsed with the cleadew dissolvingand rinsing solution and left to air dry face down on a clean tissuewhen not in use. Participants were instructed to use the lens cases for 1month, to return the lens cases to the clinic at the scheduled 1- and 3-month visits, and to use a new lens case each month.Clinical examinations of the participants’ eyes were conducted
at the baseline, 1- and 3-month scheduled visits. At each visit,
compliance with the minimum lens wear requirements and solutionregimen were verified, and subjective symptoms and feedbackwere obtained through a self-administered visual analog scalequestionnaire. Anterior ocular health, including bulbar and limbalconjunctival redness, extent of corneal and conjunctival staining,and palpebral redness and roughness were graded using theCCLRU grading scales23 using a Zeiss SL-120 biomicroscope(Carl Zeiss Meditec, Jena, Germany). The subjective ratings andocular health variables measured at baseline were considered torepresent the clinical performance of the participant’s habitual lenscare product, whereas assessments conducted at 1 and 3 monthswere representative of the cleadew cleaning and disinfecting sys-tem with the participant’s habitual contact lenses. The clinical trialwas conducted under a similar protocol to that reported previously7
with the exception that the participants used their habitual contactlenses rather than being supplied with a particular lens type.
Contact Lens Case AnalysisLens cases were collected at the 1- and 3-month visits. The lens
cases were transferred to the laboratory within 1 hr of collection foranalysis. Microbial analysis of the collected cases followed thesame protocol as described previously.14 For contact lens casesampling, swabs were taken from the inside of the contact lenscase (the case well, lid, and basket) and suspended in sterilephosphate-buffered saline. After mixing thoroughly, 400 mL ali-quots of the saline were plated onto 3 blood agar plates and 1Sabouraud agar plate. The blood agar plates were incubated aero-bically, anaerobically, or microaerophilically for 48 hr, and thenthe colonies examined. Colony morphology was recorded and eachtype of morphology was subjected to a Gram stain. The Sabouraudagar plates were incubated at 25°C for 7 days to culture for yeastand molds and the colony morphology recorded. The number ofcolony-forming units (CFU) was recorded for each colony type.For 11 participants, separate swabs were used for the different casecompartments to determine whether there were differencesbetween these sites in contamination rates or types of microbes.Identification of the types of bacteria contaminating lens cases
was performed using 16S rRNA sequencing. In brief, DNA of eachsample was extracted (using a QIAamp DNA Mini kit; Qiagen,Valencia, CA) according to the manufacturer’s instructions. Afterextraction, amplification of the 16S rRNA sequence was performedin a total volume of 25 mL containing 1 mL of DNA template, 12.5mL of EconoTaq Plus 2x Master Mix (Lucigen, Middleton, WI),10.5 mL of DNAse-free water, and 1 mL each of 10 mM universalforward primer (F27 59-AGAGTTTGATCCTGGCTCAG-39) andreverse primer (R1492; 59-CGG TTA CCT TGTTACGACTT-39).Genomic DNA of E. coli and DNAse-free water was used as thepositive and negative controls, respectively. The polymerase chainreaction was performed in a thermal cycler (Bio-Rad, Hercules,CA) at the following settings: initial denaturing at 94°C for5 min followed by 25 cycles of denaturing at 94°C for 30 sec,annealing for 30 sec at 56°C, extension at 72°C for 90 sec, anda final extension step at 72°C for 10 min. Electrophoresis of theamplified products was performed in a 1% agarose gel stained with30 ppm of GelRed 10000x solution in dimethylsulfoxide (Biotium,Hayward, CA) to ensure single bands were obtained. The poly-merase chain reaction products were then cleaned using SephadexG-50 (GE Lifescience, Uppsala, Sweden) columns and sequencedusing forward and reverse primers separately with the BigDye
TABLE 1. Details of Cleadew Cleaning and Disinfecting System
Disinfecting, Neutralizing, and CleaningTablet Dissolving and Rising Solution
Povidone–iodine (4.0 mg/tablet) Sodium borateAscorbic acid (2.0 mg/tablet) Boric acidProteolytic enzyme Sodium chloride
Hydrogen peroxide (asa preservative)
J. Tan et al. Eye & Contact Lens � Volume 0, Number 0, Month 2017
2 Eye & Contact Lens � Volume 0, Number 0, Month 2017
Copyright � Contact Lens Association of Opthalmologists, Inc. Unauthorized reproduction of this article is prohibited.
Terminator v3.1 (Applied Biosystems, Austin, TX). The sequencedsamples were purified using Sephadex G-50 columns and analyzedin an Applied Biosystems 3730 DNA Analyzer at the RamaciottiCentre for Genomics (University of New South Wales, Sydney,NSW, Australia). The sequences were manually trimmed usingSequence Scanner v1.0 software (Applied Biosystems) and theforward and the reverse sequences assembled using DNA Baserv3.5.0 (Heracle BioSoft, SRL Romania). The Basic Local Align-ment Search Tool (BLAST) of the National Center of Biotechnol-ogy Information (www.ncbi.nlm.nih.gov) database was used toidentify the aligned sequences.
Statistical Analysis of DataOne-way analysis of variance was used to compare data across
the three visits, and the level of significance was set at alpha¼0.05.Bonferroni correction was used and adjustments made for multiplecomparisons where applicable. Overall contamination rates andcontamination rates for different types of microorganisms weremeasured and tabulated.
RESULTS
Clinical Performance of thePovidone–Iodine SolutionA total of 40 participants (11 men and 29 women) with an
average age of 30613 years (range 18–60 years inclusive) wereenrolled and completed the study. However, two participants whopresented to the 3-month visit reported not having worn their con-tact lenses for 1 week before the final visit. Therefore, the 3-monthdata for these subjects were excluded from the analysis. Thirty-fourparticipants wore silicone hydrogel contact lenses, and the mostcommon lens worn was senofilcon A (by 17 participants) followedby comfilcon A (by 8 participants). Four participants routinely useda peroxide disinfection system before the study, whereas theremainder used a variety of multipurpose solutions. Table 2 de-scribes the lens/solution combinations used habitually by the par-ticipants before enrollment in the study.Ocular variables were measured for both eyes, but as there were
no differences between the eyes on statistical analysis, only data forthe left eye have been presented (Table 3). No significant differ-
ences were found between participants’ habitual lens care productat baseline compared with cleadew at the 1- or 3-month visits forbulbar and limbal conjunctival redness, extent of conjunctivalstaining, and palpebral redness and roughness (P.0.05). However,the extent of corneal staining was significantly lower when cleadewwas used at the 3-month visit compared with participants’ habituallens care product at baseline (P,0.01).No significant differences were found in subjective comfort or
vision between participants’ habitual lens care product at baselineand cleadew over the course of the study (Table 3). However, therewas a trend (P,0.1) for participants to report a significantimprovement in end-of-day comfort with cleadew at the 1- and3-month follow-up visits compared with their habitual lens careproduct (Table 3) but also a trend for slightly more itchiness duringuse of the cleadew solution.There was no case of solution-induced corneal staining with the
cleadew cleaning and disinfecting system over the course of thestudy. A total of three adverse events occurred during the study butnone were classified as serious adverse events (Table 4), and allwere deemed to be unrelated to the use of the cleadew cleaning anddisinfecting system based on histories of the events obtained byquestioning the participants. There was one possible contactlens–related corneal infiltrative event (Table 4, subject 24), butas this participant reported not wearing their contact lenses on theday the symptoms started and did not wear their contact lenses for2 weeks before the final 3-month visit, it was deemed unrelated touse of the solution. Nevertheless, should this adverse event beclassified as lens related, the rate of corneal infiltrative events per100 participant-months with cleadew was 0.83%. The adverseevent rate of cleadew with senofilcon A lenses (which containpolyvinyl pyrrolidone), the most commonly used contact lens(N¼17 participants), was zero.
Lens Case ContaminationA total of 75 lens cases were collected from the 40 study
participants (first month¼40 and third month¼35). Five subjectsdid not return their used lens cases to the final 3-month visit. Onesubject could not identify the 3-month lens storage case from the 2-month lens storage case, and one subject forgot to use a new lensstorage case after the second month. Therefore, data for these lens
TABLE 2. Habitual Lens and Disinfecting Solutions Used by Participants Before Enrollment in the Study
Contact Lens Material (Manufacturer)No. ofSubjects Disinfecting Solution (Main Disinfectant; Manufacturer)
No. ofSubjects
Senofilcon A (Johnson & Johnson Vision Care, Inc.,Jacksonville, FL)
17 AOSept (hydrogen peroxide; CIBA Vision) 3
Comfilcon A (CooperVision, Pleasanton, CA) 8 Renu Easysept (hydrogen peroxide; Bausch + Lomb, Rochester, NY) 1Lotrafilcon B (Alcon Laboratories Inc.) 5 AQuify (polyhexanide; CIBA Vision) 1Enfilcon A (CooperVision) 1 Renu (polyaminopropyl biguanide; Bausch + Lomb) 9Galyfilcon A (Johnson & Johnson Vision Care, Inc.) 1 Biotrue (polyaminopropyl biguanide and polyquaternium; Bausch + Lomb) 3Etafilcon A (Johnson & Johnson Vision Care, Inc.) 1 Complete (polyhexamethylene biguanide; Abbott Medical Optics, Santa Ana,
CA)2
Ocufilcon D (CooperVision) 1 OPTI-FREE Puremoist (polyquaternium-1 and myristamidopropyl dimethylamine;Alcon Laboratories Inc.)
10
Methafilcon A (CooperVision) 1 OPTI-FREE RepleniSH (polyquaternium-1 and myristamidopropyl dimethylamine;Alcon Laboratories Inc.)
7
Balafilcon A (Bausch + Lomb) 1 OPTI-FREE Express (polyquaternium-1 and myristamidopropyl dimethylamine;Alcon Laboratories Inc.)
1
Hilafilcon A (Bausch + Lomb) 1 Unknown 3Other hydrogels (overseas/non-English label
brands)3
Eye & Contact Lens � Volume 0, Number 0, Month 2017 Povidone–Iodine Disinfection System
� 2017 Contact Lens Association of Ophthalmologists 3
Copyright � Contact Lens Association of Opthalmologists, Inc. Unauthorized reproduction of this article is prohibited.
cases were excluded from the analysis. Of the 73 lens cases ana-lyzed, no microorganisms were cultured from 22 lens cases (30%).There was no significant difference in the contamination rates oflens cases or the type of bacteria cultured between the two visits(percentage contamination 1 month¼72.5% and at 3 month-s¼66.7%, P¼0.617); hence, the data from both visits were pooledfor analysis. The cases that were analyzed for microbial contami-nation of different compartments from 11 participants showed that,in each case, if one compartment was contaminated so was theother, and the contaminants were at similar levels and of similarcolony types (morphology and Gram stain). Similar results havebeen published previously for other contact lens multipurpose sol-utions.14 Thus, the data were combined, and all data are presentedfor total lens case.Of the 51 contaminated lens cases, 21 (42%) lens cases were
contaminated with Gram-positive bacteria only, 12 (24%) lens caseswith Gram-negative bacteria only, and 18 (35%) lens cases containedboth Gram-positive and Gram-negative bacteria. Two or morebacterial strains were cultured from 35 (69%) of the 51 contaminatedlens storage cases and 7, the maximum cultured, bacterial strainswere cultured from 1 (3%) contaminated lens case. The rate ofcontamination of cases by different microbial types is shown inFigure 1. Staphylococcus epidermidis and Serratia marcescens werethe most frequently cultured Gram-positive and Gram-negative bac-teria, respectively, from the contaminated lens storage cases (Table 5).Significantly higher numbers of Gram-negative bacteria were cul-tured from contaminated lens cases than Gram-positive bacteria(P,0.05). S. aureus (299,2936422,908 CFU/case) and Klebsiellaoxytoca (226,2566319,957 CFU/case) were cultured in the largestnumbers for Gram-positive and Gram-negative bacteria, respectively.Fungi were isolated from 8% of the cases, but no further identifica-tion work was undertaken to identify these contaminants.
DISCUSSIONThis study evaluated the cleadew cleaning and disinfecting
system in daily wear silicone hydrogel and hydrogel contact lenswearers over 3 months. This study demonstrated that cleadew iswell tolerated during contact lens wear, is associated with low
levels of corneal infiltrative events, and no cases of solution-induced corneal staining occurred over 3 months of daily wear.This is the first clinical study evaluating the rate of microbialcontamination of contact lens cases using a povidone–iodine dis-infection system. Approximately 30% of the lens storage cases hadno culturable microorganisms and, of the contaminated lens cases,approximately 65% were contaminated by a microbial type.Specific combinations of contact lenses and lens care products
have been implicated in causing greater levels of corneal stainingin both short-term evaluations after 2 to 4 hr of lens wear,24 and instudies of up to 3 months daily wear.7 In this study, no cases ofsolution-induced corneal staining were observed with cleadew insilicone hydrogel and hydrogel lens wearers over the 3-monthperiod. This shows that the cleadew cleaning and disinfecting sys-tem has potential health benefits, given that solution-induced cor-neal staining has been potentially associated with a three timesincreased risk of corneal inflammatory events.25 Indeed, only a sin-gle possible contact lens–related corneal infiltrative event occurredduring the study with cleadew (0.8% rate of corneal infiltrativeevents per 100 participant-months). This rate is lower than thosereported for polyquad (3.6%) and polyhexamethylene biguanidemultipurpose solutions (4.2%) and for a 1-step hydrogenperoxide–based system (2.2%), and is comparable with daily dis-posable lens wear (0%) in similar clinical trials.25,26 It should benoted that the reduction in corneal staining after use of cleadewcompared with the participant’s habitual lens/solution combina-tions may be affected by differences in compliance to lens anddisinfecting solution hygiene during habitual wear compared within a clinical trial. Collins and Carney27 found that complianceaffected corneal staining.Participants tended to report a clinically significant improvement
in end-of-day comfort with cleadew at the 1- and 3-month follow-upvisits (average score 85–87) compared with their habitual lens careproduct (average score 78). This may be attributed to the lack ofsolution-induced corneal staining with cleadew, as previous studieshave reported lower end-of-day comfort scores in participants withsolution-induced corneal staining compared with those without.26,28
Alternately, ocular comfort in symptomatic contact lens wearers over8 hr of lens wear can be improved by the choice of contact lens and
TABLE 3. Objective and Subjective Variables Recorded at Each Visit to the Clinic
Baseline (n¼40) 1 Month (n¼40) 3 Months (n¼38) Analysis of Variance
Clinical variable (scale ¼ 0–4)Bulbar redness—nasal 1.960.4 1.960.4 1.760.4 0.06Bulbar redness—temporal 1.960.4 2.060.4 1.860.5 0.18Bulbar redness—superior 1.660.5 1.560.3 1.460.4 0.31Bulbar redness—inferior 1.560.4 1.560.3 1.460.4 0.17Limbal redness—nasal 1.860.6 1.760.5 1.660.5 0.58Limbal redness—temporal 1.660.6 1.560.5 1.560.5 0.83Limbal redness—superior 1.960.5 1.860.4 1.760.5 0.36Limbal redness—inferior 1.960.6 1.860.5 1.860.5 0.77Corneal staining—extent (worst case) 1.161.0 0.660.7 0.560.5 <0.01Conjunctival staining—extent (worst case) 1.561.1 1.861.1 1.761.1 0.54Palpebral redness—upper lid 1.960.5 1.960.7 1.860.6 0.49Palpebral roughness—upper lid 1.160.6 0.960.6 0.960.7 0.41
Subjective rating (0–100)Comfort—insertion 9169 91610 9269 0.88Vision—insertion 89614 9469 9369 0.18Burning/stinging—insertion 93611 93612 9567 0.80Itching—insertion 9666 9765 93610 0.09Comfort—end of day 78625 87616 85615 0.08Vision—end of day 87617 89616 90612 0.76
Bold indicates significant difference (P,0.05) between visits; Italics indicates trend (P,0.1) in difference between visits.
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lens care product.29 The magnitude of the difference between com-fort at baseline compared with after 1- or 3-month use of cleadewwas greater than five points (1–100 point scale). The minimum com-fort difference that can be discerned by subjects on this scale hasbeen determined to be five points,30 indicating that, with anincreased sample size (50 in each group) there would likely bea statistical difference in comfort between the habitual multipurposedisinfecting solutions used and the cleadew solution. Although par-ticipants tended to report more itching on lens insertion when usingcleadew at the 3-month visit compared with their habitual lens careproduct at baseline, the magnitude of difference was less than 5 ona subjective rating scale of 0 to 100 and so may not be clinicallysignificant. To determine whether this difference in itchiness is sta-tistically significant, a clinical trial involving approximately 175participants in each group would need to be conducted. The differ-ence in comfort between baseline and use of cleadew may be due todifferences in compliance of participants habitually compared withwhile in a clinical trial. One study has reported that noncomplianceto lens hygiene results in lower comfort.31
This study is the first to report the rates of contamination of usedcontact lens cases while using a povidone–iodine–based disinfec-tant. Nearly 70% of the lens cases in this study were contaminatedafter use, which is similar to studies that have been conducted withcurrently available single and dual disinfectant or hydrogenperoxide–based multipurpose solutions using similar clinical trialprotocols,14,32 or a recent report of participants in a trial wherecontact lens cases were cultured after 2 weeks of use.33
The clinical trial was run under almost the same protocol asothers that have been published, including a minimum of 40
participants in each clinical trial, with the exception of not usinga defined contact lens type.7 Given contact lens type did not affectthe frequency of contamination of cases during use,14 and theculture of contact lens cases followed the same protocol as pre-vious studies,14 the data from this study has been compared withpreviously reported data. This analysis used a test of proportions tocompare between the levels of contamination of lens cases (Fig. 1).The data demonstrated that the frequency of uncontaminated lenscases with cleadew was significantly higher than cases from par-ticipants using OPTI-FREE RepleniSH (P¼0.0128; Alcon, FortWorth, TX), AQuify (P,0.0001; CIBA Vision, Atlanta, GA), orthe hydrogen peroxide solution CLEAR CARE (P¼0.0151; Alcon)but not less than when using OPTI-FREE Express (P¼0.215; Al-con). The frequency of contamination of lens cases by Gram-positive bacteria with cleadew was significantly less than withOPTI-FREE Express (P¼0.0037), AQuify (P,0.0001), orCLEAR CARE (P¼0.0006) but not less than when using OPTI-FREE RepleniSH (P¼0.0574). The level of contamination of casesby fungi when using any of the disinfecting solutions is low, butthere were significantly less fungi cultured from cleadew comparedwith CLEAR CARE lens cases (P¼0.0385) only. However, thefrequency of contamination of cleadew cases by Gram-negativebacteria was significantly higher than OPTI-FREE Express(P,0.0001) or CLEAR CARE (P¼0.0091) but not OPTI-FREERepleniSH (P¼0.234) or AQuify (P¼0.2543). When microorgan-isms isolated from the lens cases were classified as significant ornonsignificant based on their assumed pathogenicity,14 73% of thecontaminated lens cases were found to have nonsignificant levelsof microbial contaminants. These results are significantly better
TABLE 4. Adverse Events During Use of the Povidone–Iodine Solution
Subject No. Date Visit Diagnosis Eye Serious Adverse Events Product Related
12 March 30, 2015 Unscheduled—postbaseline Possible allergy or meibomian glandblockage in upper eyelid
Left No No
24 August 3, 2015 3 mo Probable infiltrative keratitis Left No No40 August 31, 2015 Unscheduled—after 1 mo Bulbar conjunctival laceration Left No No
FIG. 1. Microbial contamination ratesof cleadew compared with previouslypublished data.
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(P¼0.0178) than the 51% nonsignificant contamination rate oflens cases with OPTI-FREE RepleniSH, but not other lens cases(62%–85%).14
Willcox et al.14 demonstrated that the most commonGram-positive bacteria to contaminate contact lens cases were S.epidermidis (32%–61% of cases), Staphylococcus saprophyticus(18%–44%), S. aureus (0%–9%), and “viridans” streptococci(3%–13%), whereas the commonest Gram-negative bacteria wereDelftia acidovorans (1%–26%), Stenotrophomonas maltophilia(2%–14%), S. marcescens (0%–5%), and Achromobacter sp.(0%–10%). Cleadew cases were contaminated with S. epidermidis(12%, P¼0.0072) or S. saprophyticus (4%; P,0.0001) less fre-quently than other lens cases. There was no significant differencein contamination with S. aureus, but cleadew cases were contam-inated less frequently with viridans streptococci than those ofOPTI-FREE Express only (P¼0.0047). Cleadew cases were con-taminated less frequently with D. acidovorans (P,0.0001) or S.maltophilia (P¼0.0011) than those of OPTI-FREE RepleniSH on-ly. However, cleadew cases were contaminated more frequentlywith S. marcescens or Achromobacter sp. than those of OPTI-FREE Express (P¼0.0025 and 0.0227, respectively), CLEARCARE (P¼0.0006 and 0.0196, respectively), or AQuify(P¼0.0023 Achromobacter only). Cleadew has been shown to pro-vide excellent activity against planktonic and biofilm forms of S.
marcescens in vitro.34,35 Indeed, cleadew produced a 7.9 log10reduction in the numbers of planktonic S. marcescens ATCC13880 when tested under ISO 14729:2001 conditions.34 Cleadewproduced .4 log reduction against adherent S. marcescens on lenscases in vitro.35 It may be that a combination of contact lenses incases along with adherent S. marcescens on cases results ina reduced biocidal activity of cleadew, and this remains to be testedin future studies. It should be noted that the technique to identifythe different bacterial types in this study (16S rRNA) was differentfrom the traditional culture techniques used by Willcox et al.,14 andthis may have affected the results for different species, but not foroverall levels of Gram-positive or Gram-negative bacteria, as thosemethods were identical between the two studies (i.e., culture andGram stain).It is intriguing that there was such a low level of corneal
infiltrative events with the use of cleadew, given the relatively highfrequency of contamination of cases by Gram-negative bacteria. Aprevious study has shown a correlation between the frequency ofcontamination of lens cases by at least one or three Gram-negativebacteria (D. acidovorans, S. maltophilia, S. marcescens) and thenumber of corneal infiltrative events. Perhaps the reason for thelow level of corneal infiltrative events with cleadew was the verylow frequency of contamination with D. acidovorans, S. malto-philia, although there was a relatively high frequency of contam-ination with S. marcescens. Others have found that the risk ofa corneal infiltrative event was increased with the numbers ofcoagulase-negative staphylococci isolated from lid margins of con-tact lens wearers.36 Perhaps the low frequency of coagulase-negative staphylococci in lens cases when cleadew was used isanother reason for its low level of corneal infiltrative events.Another possible explanation involves the volume of solution inthe lens cases. The cleadew lens case can hold a volume of up to 8mL of solution, whereas the volume that can be accommodated inregular flat bottom lens cases of multipurpose solutions such asthose used in the study by Willcox et al.14 (e.g., OPTI-FREEproducts) is a maximum of 4 mL. This volume difference maydilute the bacteria (or products such as lipopolysaccharide) suchthat they are not in high enough levels to cause corneal infiltrativeevents. As all four studies reported in Willcox et al.14 and thisstudy used different participant groups, and this may affect ratesof adverse events and contact lens case contamination, a moredirect comparison between solutions using a cross-over studydesign could be used to provide further validation of the compar-isons between solutions.This study has some limitations and suggestions for further
study. The study was conducted as an open-label study designwhich may introduce bias in subjects’ responses to the question-naire. However, subjects completed a range of questions in regardto comfort and vision for various time points during the day, andthe only noteworthy finding was subjective end-of-day comfortscores. Had subjective bias been the primary causative factor, thenwe may have expected clinically and statistically significant im-provements across all the subjective responses. It may also beinteresting to enroll symptomatic subjects into a trial using cleadewto determine whether the use of this solution can improve theirsymptomatology. Discomfort during lens wear is associated withlevels of prolactin-induced protein in the tear film.37 It may bevaluable to conduct further research to evaluate whether there areany corresponding changes to tear film proteins with use of
TABLE 5. Bacterial Types Isolated From Contaminated Cleadew LensCases
Bacterial IdentificationNo. of Times Isolated(% of Lens Cases)
Colony-FormingUnits/Case(Mean6SD)
Gram-positiveBacillus aquimaris 1 (1) 1Bacillus licheniformis 1 (1) 5Brachybacterium rhamnosum 1 (1) 10Brevibacterium ammoniilyticum 1 (1) 75Enterococcus faecalis 8 (11) 1136149Kocuria kristinae 1 (1) 13Kocuria palustris 1 (1) 15Kocuria spp 1 (1) 13Microbacterium paraoxydans 1 (1) 35Microbacterium spp 1 (1) 1Micrococcus luteus 5 (7) 119,0626266,058Micrococcus spp 6 (8) 69693Propionibacterium acnes 4 (5) 1064Staphylococcus aureus 2 (3) 299,2936422,908Staphylococcus cohnii 1 (1) 20Staphylococcus epidermidis 9 (12) 33622Staphylococcus haemolyticus 3 (4) 38627Staphylococcus pasteuri 5 (7) 65699Staphylococcus saprophyticus 3 (4) 46638Staphylococcus spp 10 (13) 20620Staphylococcus warneri 8 (11) 38641Gram-negativeAcinetobacter radioresistens 2 (3) 864Acinetobacter spp 5 (7) 87,0126194,531Citrobacter freundii 1 (1) 4,783,333Citrobacter spp 1 (1) 428Enterobacter spp 5 (7) 81,2146181,002Flavobacterium lindanitolerans 1 (1) 5Klebsiella oxytoca 2 (3) 226,2566319,957Pantoea anthophila 1 (1) 8Pantoea spp 3 (4) 1736274Pseudomonas aeruginosa 2 (3) 1206163Pseudomonas japonica 1 (1) 240Pseudomonas spp 3 (4) 3268Raoultella ornithinolytica 1 (1) 350,000Serratia marcescens 9 (12) 43,0476128,857Serratia spp 2 (3) 946126
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cleadew which may be associated with the improved end-of-daycomfort scores.In conclusion, this study showed that the cleadew cleaning and
disinfecting system is compatible with a variety of siliconehydrogel and hydrogel contact lenses and has the potential toimprove subjective end-of-day comfort. Use of cleadew resulted invery low, if any, rates of corneal infiltrative events associated withlens wear. Almost three-quarters of contact lens storage casesdemonstrated nonsignificant levels of microbial contaminants, and30% of cases had no culturable microbes. Therefore, cleadewcleaning and disinfecting system may be of utility, particularly foruse among symptomatic contact lens wearers, and to reduce themicrobial burden and the potential risks of developing associatedcontact lens–related complications.
REFERENCES
1. Stapleton F, Keay L, Jalbert I, et al. The epidemiology of contact lensrelated infiltrates. Optom Vis Sci 2007;84:257–272.
2. Dumbleton K, Caffery B, Dogru M, et al. The TFOS international workshopon contact lens discomfort: Report of the subcommittee on epidemiology.Invest Ophthalmol Vis Sci 2013;54:TFOS20–TFOS36.
3. Pritchard N, Fonn D, Brazeau D. Discontinuation of contact lens wear: Asurvey. Int Contact Lens Clin 1999;26:157–162.
4. Efron N, Nichols JJ, Woods CA, et al. Trends in US contact lens prescribing2002 to 2014. Optom Vis Sci 2015;92:758–767.
5. Efron N, Morgan PB, Woods CA. Trends in Australian contact lens pre-scribing during the first decade of the 21st century (2000–2009). Clin ExpOptom 2010;93:243–252.
6. Keay L, Edwards K, Naduvilath T, et al. Factors affecting the morbidity ofcontact lens-related microbial keratitis: A population study. Invest OphthalmolVis Sci 2006;47:4302–4308.
7. Carnt NA, Evans VE, Naduvilath TJ, et al. Contact lens-related adverseevents and the silicone hydrogel lenses and daily wear care system used.Arch Ophthalmol 2009;127:1616–1623.
8. Smith AF, Orsborn G. Estimating the annual economic burden of illnesscaused by contact lens-associated corneal infiltrative events in the UnitedStates. Eye Contact Lens 2012;38:164–170.
9. Qu W, Hooymans JM, de Vries J, et al. Force analysis of bacterial trans-mission from contact lens cases to corneas, with the contact lens as theintermediary. Invest Ophthalmol Vis Sci 2011;52:2565–2570.
10. Sankaridurg PR, Sharma S, Willcox M, et al. Bacterial colonization of dispos-able soft contact lenses is greater during corneal infiltrative events than duringasymptomatic extended lens wear. J Clin Microbiol 2000;38:4420–4424.
11. Szczotka-Flynn L, Lass JH, Sethi A, et al. Risk factors for corneal infiltra-tive events during continuous wear of silicone hydrogel contact lenses.Invest Ophthalmol Vis Sci 2010;51:5421–5430.
12. Willcox M, Sharma S, Naduvilath TJ, et al. External ocular surface and lensmicrobiota in contact lens wearers with corneal infiltrates during extendedwear of hydrogel lenses. Eye Contact Lens 2011;37:90–95.
13. Willcox MD. Solutions for care of silicone hydrogel lenses. Eye ContactLens 2013;39:24–28.
14. Willcox MD, Carnt N, Diec J, et al. Contact lens case contamination duringdaily wear of silicone hydrogels. Optom Vis Sci 2010;87:456–464.
15. Kilvington S. Antimicrobial efficacy of a povidone iodine (PI) and a one-step hydrogen peroxide contact lens disinfection system. Cont Lens AnteriorEye 2004;27:209–212.
16. Martin-Navarro CM, Lorenzo-Morales J, Lopez-Arencibia A, et al. Acan-thamoeba spp.: Efficacy of Bioclen FR One Step, a povidone-iodine basedsystem for the disinfection of contact lenses. Exp Parasitol 2010;126:109–112.
17. Gatti S, Cevini C, Bruno A, et al. In vitro effectiveness of povidone-iodine onAcanthamoeba isolates from human cornea. Antimicrob Agents Chemother1998;42:2232–2234.
18. Manuj K, Gunderson C, Troupe J, et al. Efficacy of contact lens disinfectingsolutions against Staphylococcus aureus and Pseudomonas aeruginosa. EyeContact Lens 2006;32:216–218.
19. Yanai R, Yamada N, Ueda K, et al. Evaluation of povidone-iodine asa disinfectant solution for contact lenses: Antimicrobial activity and cyto-toxicity for corneal epithelial cells. Cont Lens Anterior Eye 2006;29:85–91.
20. Demirbilek M, Evren E. Efficacy of multipurpose contact lens solutionsagainst ESBL-positive Escherichia coli, MRSA, and Candida albicans clin-ical isolates. Eye Contact Lens 2014;40:157–160.
21. Kilvington S, Lam A, Nikolic M, et al. Resistance and growth of Fusariumspecies in contact lens disinfectant solutions. Optom Vis Sci 2013;90:430–438.
22. Kobayashi T, Gibbon L, Mito T, et al. Efficacy of commercial soft contactlens disinfectant solutions against Acanthamoeba. Jpn J Ophthalmol 2011;55:547–557.
23. Terry RL, Schnider CM, Holden BA, et al. CCLRU standards for success ofdaily and extended wear contact lenses. Optom Vis Sci 1993;70:234–243.
24. Andrasko G, Ryen K. Corneal staining and comfort observed with tradi-tional and silicone hydrogel lenses and multipurpose solution combinations.Optometry 2008;79:444–454.
25. Carnt N, Jalbert I, Stretton S, et al. Solution toxicity in soft contact lensdaily wear is associated with corneal inflammation. Optom Vis Sci 2007;84:309–315.
26. Lazon de la Jara P, Papas E, Diec J, et al. Effect of lens care systems on theclinical performance of a contact lens. Optom Vis Sci 2013;90:344–350.
27. Collins MJ, Carney LG. Compliance with care and maintenance proceduresamongst contact lens wearers. Clin Exp Optom 1986;69:174–177.
28. Diec J, Evans VE, Tilia D, et al. Comparison of ocular comfort, vision, andSICS during silicone hydrogel contact lens daily wear. Eye Contact Lens2012;38:2–6.
29. Tilia D, Lazon de la Jara P, Peng N, et al. Effect of lens and solution choiceon the comfort of contact lens wearers. Optom Vis Sci 2013;90:411–418.
30. Papas EB, Keay L, Golebiowski B. Estimating a just-noticeable differencefor ocular comfort in contact lens wearers. Invest Ophthalmol Vis Sci 2011;52:4390–4394.
31. Dumbleton K, Woods C, Jones L, et al. Comfort and vision with siliconehydrogel lenses: Effect of compliance. Optom Vis Sci 2010;87:421–425.
32. Tilia D, Lazon de la Jara P, Zhu H, et al. The effect of compliance oncontact lens case contamination. Optom Vis Sci 2014;91:262–271.
33. Dantam J, McCanna DJ, Subbaraman LN, et al. Microbial contamination ofcontact lens storage cases during daily wear use. Optom Vis Sci 2016;93:925–932.
34. Vijay AK, Liu L, Ly TCN, et al. Efficacy a novel povidone iodine basedcontact lens disinfection system against bacterial biofilm. Invest OphthalmolVis Sci 2016;57: E-Abstract 1454.
35. Hotta F, Eguchi H, Miyamoto T, et al. Efficacy of povidone-iodine fordisinfection of bacteria in the contact lens storage cases. Invest OphthalmolVis Sci 2011;52: E-Abstract 5838.
36. Szczotka-Flynn L, Jiang Y, Raghupathy S, et al. Corneal inflammatoryevents with daily silicone hydrogel lens wear. Optom Vis Sci 2014;91:3–12.
37. Masoudi S, Stapleton FJ, Willcox MD. Contact lens-induced discomfort andprotein changes in tears. Optom Vis Sci 2016;93:955–962.
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